Isolated Complex Endophyte Compositions and Methods for Improved Plant Traits

ABSTRACT

This invention relates to methods and materials for providing a benefit to a plant by associating the plant with a complex endophyte comprising a host fungus further comprising a component bacterium, including benefits to a plant derived from a seed or other plant element treated with a complex endophyte. For example, this invention provides purified complex endophytes, purified complex endophyte components such as bacteria or fungi, synthetic combinations comprising said complex endophytes and/or components, and methods of making and using the same.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.16/221,262, filed Dec. 14, 2018, which is a continuation of U.S.application Ser. No. 15/143,398, filed Apr. 29, 2016, which claims thebenefit of U.S. Provisional Application No. 62/156,001, filed May 1,2015, which is hereby incorporated in its entirety by reference.

SEQUENCE LISTING

The instant application contains a Sequence Listing with 333 sequenceswhich has been submitted via EFS-Web and is hereby incorporated byreference in its entirety. Said ASCII copy, created on Jun. 15, 2021, isnamed IAI-038C2_sequencelisting.txt, and is 512,967 bytes in size.

FIELD OF THE INVENTION

This invention relates to compositions and methods for improving thecultivation of plants, particularly agricultural plants such as maize,wheat, barley, sorghum, millet, rice, soybean, canola, rapeseed, cotton,alfalfa, sugarcane, cassava, potato, tomato, and vegetables. Forexample, this invention describes fungal endophytes that compriseadditional components, such as bacteria, that may be used to impartimproved agronomic traits to plants. The disclosed invention alsodescribes methods of improving plant characteristics by introducingfungal endophytes that comprise additional components to those plants.Further, this invention also provides methods of treating seeds andother plant parts with fungal endophytes that further compriseadditional components, to impart improved agronomic characteristics toplants, particularly agricultural plants.

BACKGROUND OF THE INVENTION

According the United Nations Food and Agricultural Organization (UNFAO), the world's population will exceed 9.6 billion people by the year2050, which will require significant improvements in agriculture to meetgrowing food demands. At the same time, conservation of resources (suchas water, land), reduction of inputs (such as fertilizer, pesticides,herbicides), environmental sustainability, and climate change areincreasingly important factors in how food is grown. There is a need forimproved agricultural plants and farming practices that will enable theneed for a nearly doubled food production with fewer resources, moreenvironmentally sustainable inputs, and with plants with improvedresponses to various biotic and abiotic stresses (such as pests,drought, disease).

Today, crop performance is optimized primarily via technologies directedtowards the interplay between crop genotype (e.g., plant breeding,genetically-modified (GM) crops) and its surrounding environment (e.g.,fertilizer, synthetic herbicides, pesticides). While these paradigmshave assisted in doubling global food production in the past fiftyyears, yield growth rates have stalled in many major crops and shifts inthe climate have been linked to production instability and declines inimportant crops, driving an urgent need for novel solutions to cropyield improvement. In addition to their long development and regulatorytimelines, public fears of GM-crops and synthetic chemicals havechallenged their use in many key crops and countries, resulting in alack of acceptance for many GM traits and the exclusion of GM crops andmany synthetic chemistries from some global markets. Thus, there is asignificant need for innovative, effective, environmentally-sustainable,and publically-acceptable approaches to improving the yield andresilience of crops to stresses.

Improvement of crop resilience to biotic and abiotic stresses has provenchallenging for conventional genetic and chemical paradigms for cropimprovement. This challenge is in part due to the complex, network-levelchanges that arise during exposure to these stresses. For example,plants under stress can succumb to a variety of physiological anddevelopmental damages, including dehydration, elevated reactive oxygenspecies, impairment of photosynthetic carbon assimilation, inhibition oftranslocation of assimilates, increased respiration, reduced organ sizedue to a decrease in the duration of developmental phases, disruption ofseed development, and a reduction in fertility.

Like humans, who utilize a complement of beneficial microbial symbionts,plants have been purported to derive a benefit from the vast array ofbacteria and fungi that live both within and around their tissues inorder to support the plant's health and growth. Endophytes are symbioticorganisms (typically bacteria or fungi) that live within plants, andinhabit various plant tissues, often colonizing the intercellular spacesof host leaves, stems, flowers, fruits, seeds, or roots. To date, asmall number of symbiotic endophyte-host relationships have beenanalyzed in limited studies to provide fitness benefits to model hostplants within controlled laboratory settings, such as enhancement ofbiomass production and nutrition, increased tolerance to stress such asdrought and pests. There is still a need to develop betterplant-endophyte systems to confer benefits to a variety ofagriculturally-important plants such as maize and soybean, for exampleto provide improved yield and tolerance to the environmental stressespresent in many agricultural situations for such agricultural plants.

There are very few examples of “complex endophytes”, or endophytesfurther comprising another component (such as a virus, or a bacterium),that have been described in the literature, including: a survey ofcupressaceous trees (Hoffman and Arnold, 2010 Appl. Environ. Microbiol.76: 4063-4075, incorporated herein by reference in its entirety) and onespecies of tropical grasses (Marquez et al., 2007 Science 315: 513-515).Desire et al. (2014 ISME J. 8: 257-270, incorporated herein by referencein its entirety) describe the existence of more than one species ofbacteria residing within a fungal endophyte. It has been demonstratedthat at least one of these endofungal bacteria is able to produce aplant hormone that enhances plant growth and others can producesubstances with anti-cancer and anti-malaria properties (Hoffman et al.,2013 PLOS One 8: e73132; Jung and Arnold, 2012 The Effects of EndohyphalBacteria on Anti-Cancer and Anti-Malaria Metabolites of EndophyticFungi, Honors Thesis, University of Arizona, incorporated herein byreference in their entirety). However, these complex endophytes have notbeen shown to exist in cultivated plants of agricultural importance suchas maize, soybean, wheat, cotton, rice, etc. As such, the complexendophytes, or bacteria isolated from such complex endophytes, have notpreviously been conceived as a viable mechanism to address the need toprovide improved yield and tolerance to environmental stresses forplants of agricultural importance.

Thus, there is a need for compositions and methods of providingagricultural plants with improved yield and tolerance to various bioticand abiotic stresses. Provided herein are novel compositions of complexendophytes, formulations of complex endophytes for treatment of plantsand plant parts, novel complex endophyte-plant compositions, and methodsof use for the same, created based on the analysis of the key propertiesthat enhance the utility and commercialization of a complex endophytecomposition.

SUMMARY OF THE INVENTION

Disclosed herein is a synthetic composition, comprising a plant elementheterologously associated with a complex endophyte, wherein the complexendophyte is capable of providing a trait of agronomic importance to theplant element.

In some embodiments, the trait of agronomic importance is selected fromthe group consisting of: altered oil content, altered protein content,altered seed carbohydrate composition, altered seed oil composition,altered seed protein composition, increased chemical tolerance,increased cold tolerance, delayed senescence, increased diseaseresistance, increased drought tolerance, increased ear weight, growthimprovement, health enhancement, increased heat tolerance, increasedherbicide tolerance, increased herbivore resistance, improved nitrogenfixation, improved nitrogen utilization, improved nutrient useefficiency, improved root architecture, improved water use efficiency,increased biomass, increased root length, increased seedling rootlength, germination rate, increased seed weight, increased shoot length,increased seedling shoot length, increased shoot biomass, increasedyield, increased yield under water-limited conditions, increased kernelmass, improved kernel moisture content, increased metal tolerance,increased number of ears, increased number of kernels per ear, increasednumber of pods, nutrition enhancement, improved pathogen resistance,improved pest resistance, photosynthetic capability improvement,salinity tolerance, stay-green, vigor improvement, increased dry weightof mature seeds, increased fresh weight of mature seeds, increasednumber of mature seeds per plant, increased chlorophyll content,increased seed germination, increased number of pods per plant,increased length of pods per plant, reduced number of wilted leaves perplant, reduced number of severely wilted leaves per plant, increasednumber of non-wilted leaves per plant, increased plant height, earlieror increased flowering, increased protein content, increased fermentablecarbohydrate content, reduced lignin content, male sterility, andincreased antioxidant content. In some embodiments, trait of agronomicimportance is selected from the group consisting of: germination rate,emergence rate, shoot biomass, root biomass, seedling root length,seedling shoot length, and yield.

In some embodiments, the synthetic composition further comprises anagronomic formulation that further comprises one or more of thefollowing: a stabilizer, or a preservative, or a carrier, or asurfactant, or an anticomplex agent, fungicide, nematicide, bactericide,insecticide, and herbicide, or any combination thereof. In someembodiments, the complex endophyte is present in an amount of at leastabout 10{circumflex over ( )}2 CFU per plant element.

In some embodiments, the synthetic compositions described hereincomprise a complex endophyte comprising a host fungus from a classselected from the group consisting of: Dothideomycetes, Sordariomycetes,or any of the corresponding anamorph or telomorph taxonomy of thepreceding; and/or a bacterium from a class selected from the groupconsisting of: Bacilli, Betaproteobacteria, Gammaproteobacteria; and/ora host fungus from an order selected from the group consisting of:Botryosphaeriales, Dothideales, Pleosporales, Coniochateles, Xylariales,or any of the corresponding anamorph or telomorph taxonomy of thepreceding; and/or a bacterium from an order selected from the groupconsisting of: Bacillales, Burkholderiales, Enterobacteriales,Xanthomonadales.

10. The synthetic composition of any of claims 1-5, wherein the complexendophyte comprises a host fungus from a family selected from the groupconsisting of: Botryosphaeriaceae, Dothioraceae, Montagnulacea,Pleosporacea, Coniochaetaceae, Amphisphaeriaceae, Xylariacea, or any ofthe corresponding anamorph or telomorph taxonomy of the preceding;and/or a bacterium from a family selected from the group consisting of:Bacillaceae, Burkholderiaceae, Enterobacteriaceae, Xanthomonadaceae;and/or a host fungus from a genus selected from the group consisting of:Boryosphaeria, Microdiplodia, Pestalotiopsis, Phyllosticta, Alternaria,Lecythophora, Daldinia, or any of the corresponding anamorph ortelomorph taxonomy of the preceding; and/or a bacterium from a genusselected from the group consisting of: Dyella, Pantoea, Luteibacter,Ralstonia, Erwinia, Bacillus; and/or a nucleic acid sequence at least95% identical to a nucletic acid sequence selected from the groupconsisting of SEQ ID NO: 1 through SEQ ID NO: 333; and/or is selectedfrom those listed in Table 4.

In some embodiments, the complex endophyte is associated with a plantelement but is not directly contacting the plant element.

In some embodiments, the plant element is selected from the groupconsisting of: whole plant, seedling, meristematic tissue, groundtissue, vascular tissue, dermal tissue, seed, leaf, root, shoot, stem,flower, fruit, stolon, bulb, tuber, corm, keikis, and bud. In someembodiments, the the plant element is from a plant selected from thegroup consisting of: wheat, soybean, maize, cotton, canola, barley,sorghum, millet, rice, rapeseed, alfalfa, tomato, sugarbeet, sorghum,almond, walnut, apple, peanut, strawberry, lettuce, orange, potato,banana, sugarcane, potato, cassava, mango, guava, palm, onions, olives,peppers, tea, yams, cacao, sunflower, asparagus, carrot, coconut, lemon,lime, barley, watermelon, cabbage, cucumber, grape, and turfgrass.

Also disclosed herein is a plurality of the synthetic compositionsdescribed herein, e.g., confined within an object selected from thegroup consisting of: bottle, jar, ampule, package, vessel, bag, box,bin, envelope, carton, container, silo, shipping container, truck bed,and case; and/or placed in a medium that promotes plant growth, themedium selected from the group consisting of: soil, hydroponicapparatus, and artificial growth medium, e.g., the medium is soil,wherein the synthetic compositions are placed in the soil withsubstantially equal spacing between each seed; and/or wherein thesynthetic compositions are shelf-stable.

Also disclosed herein is a plant grown from the synthetic combinationsdescribed herein, wherein the plant exhibits an improved phenotype ofagronomic interest, selected from the group consisting of: altered oilcontent, altered protein content, altered seed carbohydrate composition,altered seed oil composition, altered seed protein composition,increased chemical tolerance, increased cold tolerance, delayedsenescence, increased disease resistance, increased drought tolerance,increased ear weight, growth improvement, health enhancement, increasedheat tolerance, increased herbicide tolerance, increased herbivoreresistance, improved nitrogen fixation, improved nitrogen utilization,improved nutrient use efficiency, improved root architecture, improvedwater use efficiency, increased biomass, increased root length,increased seedling root length, germination rate, increased seed weight,increased shoot length, increased seedling shoot length, increased shootbiomass, increased yield, increased yield under water-limitedconditions, increased kernel mass, improved kernel moisture content,increased metal tolerance, increased number of ears, increased number ofkernels per ear, increased number of pods, nutrition enhancement,improved pathogen resistance, improved pest resistance, photosyntheticcapability improvement, salinity tolerance, stay-green, vigorimprovement, increased dry weight of mature seeds, increased freshweight of mature seeds, increased number of mature seeds per plant,increased chlorophyll content, increased seed germination, increasednumber of pods per plant, increased length of pods per plant, reducednumber of wilted leaves per plant, reduced number of severely wiltedleaves per plant, increased number of non-wilted leaves per plant,increased plant height, earlier or increased flowering, increasedprotein content, increased fermentable carbohydrate content, reducedlignin content, male sterility, and increased antioxidant content.

Also disclosed herein is a plant, plant element, or progeny of the plantgrown from the synthetic combinations described herein wherein the plantor progeny of the plant comprises in at least one of its plant elementsthe complex endophyte, fungal host, or bacterial component.

Also disclosed herein is a method of inoculating a plant with a fungalendophyte, comprising contacting a plant element of the plant with aformulation comprising a heterologous complex endophyte, wherein thecomplex endophyte comprises the fungal endophyte and a method ofinoculating a plant with a bacterial endophyte, comprising contacting aplant element of the plant with a formulation comprising a heterologouscomplex endophyte, wherein the complex endophyte comprises the bacterialendophyte. In some embodiments, the inoculation improves a trait ofagronomic importance in the plant.

Also disclosed herein is a method of improving a trait of agronomicimportance in a plant, comprising contacting a plant element with aformulation comprising a heterologous complex endophyte; as compared toan isoline plant grown from a plant reproductive element not associatedwith the complex endophyte and a method of improving a trait ofagronomic importance in a plant, comprising growing the plant from aplant reproductive element that has been contacted with a formulationcomprising a heterologous complex endophyte; as compared to an isolineplant grown from a plant reproductive element not associated with thecomplex endophyte. In some embodiments, the complex endophyte comprisesa bacterium within a host fungus. In some embodiments, the complexendophyte comprises a fungus within a host fungus

Also disclosed herein is a method of improving a trait of agronomicimportance in a plant, comprising growing the plant from a plantreproductive element that has been contacted with a formulationcomprising a heterologous complex endophyte, wherein the complexendophyte comprises a bacterium within a host fungus; as compared to anisoline plant grown from a plant reproductive element not associatedwith the bacterium and a method of improving a trait of agronomicimportance in a plant, comprising growing the plant from a plantreproductive element that has been contacted with a formulationcomprising a heterologous complex endophyte, wherein the complexendophyte comprises a fungus within a host fungus; as compared to anisoline plant grown from a plant reproductive element not associatedwith the fungus. In some embodiments, the trait of agronomic importanceis selected from the group consisting of: altered oil content, alteredprotein content, altered seed carbohydrate composition, altered seed oilcomposition, altered seed protein composition, increased chemicaltolerance, increased cold tolerance, delayed senescence, increaseddisease resistance, increased drought tolerance, increased ear weight,growth improvement, health enhancement, increased heat tolerance,increased herbicide tolerance, increased herbivore resistance, improvednitrogen fixation, improved nitrogen utilization, improved nutrient useefficiency, improved root architecture, improved water use efficiency,increased biomass, increased root length, increased seedling rootlength, germination rate, increased seed weight, increased shoot length,increased seedling shoot length, increased shoot biomass, increasedyield, increased yield under water-limited conditions, increased kernelmass, improved kernel moisture content, increased metal tolerance,increased number of ears, increased number of kernels per ear, increasednumber of pods, nutrition enhancement, improved pathogen resistance,improved pest resistance, photosynthetic capability improvement,salinity tolerance, stay-green, vigor improvement, increased dry weightof mature seeds, increased fresh weight of mature seeds, increasednumber of mature seeds per plant, increased chlorophyll content,increased seed germination, increased number of pods per plant,increased length of pods per plant, reduced number of wilted leaves perplant, reduced number of severely wilted leaves per plant, increasednumber of non-wilted leaves per plant, increased plant height, earlieror increased flowering, increased protein content, increased fermentablecarbohydrate content, reduced lignin content, male sterility, andincreased antioxidant content. In some embodiments, the trait ofagronomic importance is selected from the group consisting of:germination rate, emergence rate, shoot biomass, seedling root length,seedling shoot length, and yield. In some embodiments, the trait ofagronomic importance is improved under normal watering conditions. Insome embodiments, the the trait of agronomic importance is improvedunder conditions of water limitation. In some embodiments, the plantreproductive element is a seed from a soybean plant, and wherein thecomplex endophyte comprises a fungus of the genus Dothideomyetes. Insome embodiments, the plant reproductive element is a seed from a wheatplant, and wherein the complex endophyte comprises a fungus of the genusSodariomycetes. In some embodiments, the complex endophyte is present inthe formulation in an amount capable of modulating at least one of: atrait of agronomic importance, the transcription of a gene, theexpression of a protein, the level of a hormone, the level of ametabolite, and the population of endogenous microbes in plants grownfrom the seeds, as compared to isoline plants not associated with, orgrown from plant elements associated with, the complex endophyte. Insome embodiments, the agronomic formulation further comprises one ormore of the following: a stabilizer, or a preservative, or a carrier, ora surfactant, or an anticomplex agent, fungicide, nematicide,bactericide, insecticide, and herbicide, or any combination thereof.

In some embodiments of any of the methods described herein, the complexendophyte is present in an amount of at least about 10{circumflex over( )}2 CFU per plant element.

In some embodiments of any of the methods described herein, the complexendophyte comprises a host fungus from a class selected from the groupconsisting of: Dothideomycetes, Sordariomycetes, or any of thecorresponding anamorph or telomorph taxonomy of the preceding; and/or abacterium from a class selected from the group consisting of: Bacilli,Betaproteobacteria, Gammaproteobacteria; and/or a host fungus from anorder selected from the group consisting of: Botryosphaeriales,Dothideales, Pleosporales, Coniochateles, Xylariales, or any of thecorresponding anamorph or telomorph taxonomy of the preceding; and/or abacterium from an order selected from the group consisting of:Bacillales, Burkholderiales, Enterobacteriales, Xanthomonadales; and/ora host fungus from a family selected from the group consisting of:Botryosphaeriaceae, Dothioraceae, Montagnulacea, Pleosporacea,Coniochaetaceae, Amphisphaeriaceae, Xylariacea, or any of thecorresponding anamorph or telomorph taxonomy of the preceding; and/or abacterium from a family selected from the group consisting of:Bacillaceae, Burkholderiaceae, Enterobacteriaceae, Xanthomonadaceae;and/or a host fungus from a genus selected from the group consisting of:Boryosphaeria, Microdiplodia, Pestalotiopsis, Phyllosticta, Alternaria,Lecythophora, Daldinia, or any of the corresponding anamorph ortelomorph taxonomy of the preceding; and/or a bacterium from a genusselected from the group consisting of: Dyella, Pantoea, Luteibacter,Ralstonia, Erwinia, Bacillus; and/or a nucleic acid sequence at least95% identical to a nucletic acid sequence selected from the groupconsisting of SEQ ID NO: 1 through SEQ ID NO: 333; and/or is selectedfrom those listed in Table 4.

In some embodiments of any of the methods described herein, the complexendophyte is associated with a plant element but is not directlycontacting the plant element. In some embodiments of any of the methodsdescribed herein, the plant element is selected from the groupconsisting of: whole plant, seedling, meristematic tissue, groundtissue, vascular tissue, dermal tissue, seed, leaf, root, shoot, stem,flower, fruit, stolon, bulb, tuber, corm, keikis, and bud. n someembodiments of any of the methods described herein, the plant element isfrom a plant selected from the group consisting of: wheat, soybean,maize, cotton, canola, barley, sorghum, millet, rice, rapeseed, alfalfa,tomato, sugarbeet, sorghum, almond, walnut, apple, peanut, strawberry,lettuce, orange, potato, banana, sugarcane, potato, cassava, mango,guava, palm, onions, olives, peppers, tea, yams, cacao, sunflower,asparagus, carrot, coconut, lemon, lime, barley, watermelon, cabbage,cucumber, grape, and turfgrass.

Also disclosed herein is a plant element from the plant produced by anyof the methods described herein.

Also disclosed herein is a method of improving a trait of agronomicimportance in a plant, comprising isolating a bacterial endophyte from acomplex endophyte, and growing the plant from a plant reproductiveelement onto which the bacterial endophyte is heterologously disposed;as compared to an isoline plant grown from a plant reproductive elementnot associated with the bacterial endophyte. In some embodiments, thetrait of agronomic importance is selected from the group consisting of:altered oil content, altered protein content, altered seed carbohydratecomposition, altered seed oil composition, altered seed proteincomposition, increased chemical tolerance, increased cold tolerance,delayed senescence, increased disease resistance, increased droughttolerance, increased ear weight, growth improvement, health enhancement,increased heat tolerance, increased herbicide tolerance, increasedherbivore resistance, improved nitrogen fixation, improved nitrogenutilization, improved nutrient use efficiency, improved rootarchitecture, improved water use efficiency, increased biomass,increased root length, increased seedling root length, germination rate,increased seed weight, increased shoot length, increased seedling shootlength, increased shoot biomass, increased yield, increased yield underwater-limited conditions, increased kernel mass, improved kernelmoisture content, increased metal tolerance, increased number of ears,increased number of kernels per ear, increased number of pods, nutritionenhancement, improved pathogen resistance, improved pest resistance,photosynthetic capability improvement, salinity tolerance, stay-green,vigor improvement, increased dry weight of mature seeds, increased freshweight of mature seeds, increased number of mature seeds per plant,increased chlorophyll content, increased seed germination, increasednumber of pods per plant, increased length of pods per plant, reducednumber of wilted leaves per plant, reduced number of severely wiltedleaves per plant, increased number of non-wilted leaves per plant,increased plant height, earlier or increased flowering, increasedprotein content, increased fermentable carbohydrate content, reducedlignin content, male sterility, and increased antioxidant content. Insome embodiments, the trait of agronomic importance is selected from thegroup consisting of: germination rate, emergence rate, shoot biomass,seedling root length, seedling shoot length, and yield. In someembodiments, he trait of agronomic importance is improved under normalwatering conditions. In some embodiments, the trait of agronomicimportance is improved under conditions of water limitation. In someembodiments, the complex endophyte comprises a host fungus from a classselected from the group consisting of: Dothideomycetes, Sordariomycetes,or any of the corresponding anamorph or telomorph taxonomy of thepreceding; and/or a bacterium from a class selected from the groupconsisting of: Bacilli, Betaproteobacteria, Gammaproteobacteria; and/ora host fungus from an order selected from the group consisting of:Botryosphaeriales, Dothideales, Pleosporales, Coniochateles, Xylariales,or any of the corresponding anamorph or telomorph taxonomy of thepreceding; and/or a bacterium from an order selected from the groupconsisting of: Bacillales, Burkholderiales, Enterobacteriales,Xanthomonadales; and/or a host fungus from a family selected from thegroup consisting of: Botryosphaeriaceae, Dothioraceae, Montagnulacea,Pleosporacea, Coniochaetaceae, Amphisphaeriaceae, Xylariacea, or any ofthe corresponding anamorph or telomorph taxonomy of the preceding;and/or a bacterium from a family selected from the group consisting of:Bacillaceae, Burkholderiaceae, Enterobacteriaceae, Xanthomonadaceae;and/or a host fungus from a genus selected from the group consisting of:Boryosphaeria, Microdiplodia, Pestalotiopsis, Phyllosticta, Alternaria,Lecythophora, Daldinia, or any of the corresponding anamorph ortelomorph taxonomy of the preceding; and/or a bacterium from a genusselected from the group consisting of: Dyella, Pantoea, Luteibacter,Ralstonia, Erwinia, Bacillus; and/or a nucleic acid sequence at least95% identical to a nucletic acid sequence selected from the groupconsisting of SEQ ID NO: 1 through SEQ ID NO: 333.

Also disclosed herein is a plant produced by any of the methodsdescribed herein.

Also disclosed herein is a method for preparing a synthetic composition,comprising associating the surface of a plurality of plant elements witha formulation comprising a purified microbial population that comprisesa complex endophyte that is heterologous to the seed, wherein thecomplex endophyte is present in the formulation in an amount capable ofmodulating at least one of: a trait of agronomic importance, thetranscription of a gene, the expression of a protein, the level of ahormone, the level of a metabolite, and the population of endogenousmicrobes in plants grown from the seeds, as compared to isoline plantsnot associated with, or grown from plant elements associated with, theformulation. In some embodiments, the trait of agronomic importance isselected from the group consisting of: altered oil content, alteredprotein content, altered seed carbohydrate composition, altered seed oilcomposition, altered seed protein composition, increased chemicaltolerance, increased cold tolerance, delayed senescence, increaseddisease resistance, increased drought tolerance, increased ear weight,growth improvement, health enhancement, increased heat tolerance,increased herbicide tolerance, increased herbivore resistance, improvednitrogen fixation, improved nitrogen utilization, improved nutrient useefficiency, improved root architecture, improved water use efficiency,increased biomass, increased root length, increased seedling rootlength, germination rate, increased seed weight, increased shoot length,increased seedling shoot length, increased shoot biomass, increasedyield, increased yield under water-limited conditions, increased kernelmass, improved kernel moisture content, increased metal tolerance,increased number of ears, increased number of kernels per ear, increasednumber of pods, nutrition enhancement, improved pathogen resistance,improved pest resistance, photosynthetic capability improvement,salinity tolerance, stay-green, vigor improvement, increased dry weightof mature seeds, increased fresh weight of mature seeds, increasednumber of mature seeds per plant, increased chlorophyll content,increased seed germination, increased number of pods per plant,increased length of pods per plant, reduced number of wilted leaves perplant, reduced number of severely wilted leaves per plant, increasednumber of non-wilted leaves per plant, increased plant height, earlieror increased flowering, increased protein content, increased fermentablecarbohydrate content, reduced lignin content, male sterility, andincreased antioxidant content. In some embodiments, the trait ofagronomic importance is selected from the group consisting of:germination rate, emergence rate, shoot biomass, seedling root length,seedling shoot length, and yield. In some embodiments, the trait ofagronomic importance is improved under normal watering conditions. Insome embodiments, the trait of agronomic importance is improved underconditions of water limitation.

In some embodiments of the methods, the synthetic composition used inthe methods described herein further comprises an agronomic formulationthat further comprises one or more of the following: a stabilizer, or apreservative, or a carrier, or a surfactant, or an anticomplex agent,fungicide, nematicide, bactericide, insecticide, and herbicide, or anycombination thereof.

In some embodiments of the methods, the complex endophyte is present inan amount of at least about 10{circumflex over ( )}2 CFU per plantelement; and/or the complex endophyte comprises a host fungus from aclass selected from the group consisting of: Dothideomycetes,Sordariomycetes, or any of the corresponding anamorph or telomorphtaxonomy of the preceding; and/or a bacterium from a class selected fromthe group consisting of: Bacilli, Betaproteobacteria,Gammaproteobacteria; and/or a host fungus from an order selected fromthe group consisting of: Botryosphaeriales, Dothideales, Pleosporales,Coniochateles, Xylariales, or any of the corresponding anamorph ortelomorph taxonomy of the preceding; and/or a bacterium from an orderselected from the group consisting of: Bacillales, Burkholderiales,Enterobacteriales, Xanthomonadales; and/or a host fungus from a familyselected from the group consisting of: Botryosphaeriaceae, Dothioraceae,Montagnulacea, Pleosporacea, Coniochaetaceae, Amphisphaeriaceae,Xylariacea, or any of the corresponding anamorph or telomorph taxonomyof the preceding; and/or a bacterium from a family selected from thegroup consisting of: Bacillaceae, Burkholderiaceae, Enterobacteriaceae,Xanthomonadaceae; and/or a host fungus from a genus selected from thegroup consisting of: Boryosphaeria, Microdiplodia, Pestalotiopsis,Phyllosticta, Alternaria, Lecythophora, Daldinia, or any of thecorresponding anamorph or telomorph taxonomy of the preceding; and/or abacterium from a genus selected from the group consisting of: Dyella,Pantoea, Luteibacter, Ralstonia, Erwinia, Bacillus; and/or a nucleicacid sequence at least 95% identical to a nucletic acid sequenceselected from the group consisting of SEQ ID NO: 1 through SEQ ID NO:333; and/or the complex endophyte is selected from those listed in Table4.

In some embodiments of the methods, the complex endophyte is associatedwith a plant element but is not directly contacting the plant element.In some embodiments of the methods, the plant element is selected fromthe group consisting of: whole plant, seedling, meristematic tissue,ground tissue, vascular tissue, dermal tissue, seed, leaf, root, shoot,stem, flower, fruit, stolon, bulb, tuber, corm, keikis, and bud. In someembodiments of the methods, the plant element is from a plant selectedfrom the group consisting of: wheat, soybean, maize, cotton, canola,barley, sorghum, millet, rice, rapeseed, alfalfa, tomato, sugarbeet,sorghum, almond, walnut, apple, peanut, strawberry, lettuce, orange,potato, banana, sugarcane, potato, cassava, mango, guava, palm, onions,olives, peppers, tea, yams, cacao, sunflower, asparagus, carrot,coconut, lemon, lime, barley, watermelon, cabbage, cucumber, grape, andturfgrass.

Also described herein is a method of improving the efficacy of abacterial endophyte in an application, comprising utilizing a complexendophyte, wherein the complex endophyte comprises the bacterialendophyte and a method of improving the efficacy of a fungal endophytein an application, comprising utilizing a complex endophyte, wherein thecomplex endophyte comprises the fungal endophyte. In some embodiments,the application is selected from the group consisting of: agriculture,plant improvement, water quality improvement, snow or ice production,bioremediation, industrial compound production, pharmaceutical compoundproduction, and production of bioengineered substances. In someembodiments, the application is a production method of a compositionbelonging to a class of compound selected from the group consisting of:acids, alcohols, amino acids, amylases, antibiotics, biogases,bioplastics, citric acid, enzymes, esters, fatty acids, flavoringagents, glutamic acid, human or animal hormones, human growth hormone,ice, insulin, lactic acid, lipases, lipids, minerals, nitrogen, oils,nucleic acids, pectinases, preservatives, proteins, snow, sugars,vaccines, viruses, vitamins, and waxes.

Also disclosed herein is a method of improving the performance of abacterial endophyte in an application, comprising identifying a complexendophyte comprising a bacterium comprising a nucleic acid sequence withat least 95% identity to that of the bacterial endophyte, andsubstituting the complex endophyte for the bacterial endophyte in theapplication. In some embodiments, the bacterial endophyte is furtherassociated with a plant element, e.g., a Gram-negative bacterialendophyte. In some embodiments, the characteristic is selected from thegroup consisting of: efficacy, survivability, shelf-stability, toleranceto an antibiotic, tolerance to reduced environmental moisture.

DESCRIPTION OF THE DRAWINGS

FIG. 1: complex endophyte and component bacterial culture phentoypiccharacteristics.

FIG. 2A and FIG. 2B: wheat greenhouse emergence rates. Spring wheatplants (Variety 1, FIG. 2A; Variety 2, FIG. 2B) grown from seeds treatedwith the complex endophyte SYM166 demonstrated an improved averageemergence rate in greenhouse experiments, as compared to plants treatedwith the formulation control and plants treated with non-complex fungalendophytes. Particular improvement was seen in early emergence rates.

FIG. 3A and FIG. 3B: wheat greenhouse dry shoot biomass. Spring wheatplants (Variety 1, FIG. 3A; Variety 2, FIG. 3B) grown from seeds treatedwith the complex endophyte SYM166 demonstrated an improved average wheatdry shoot biomass in greenhouse experiments, as compared to plantstreated with the formulation control and plants treated with non-complexfungal endophytes.

FIG. 4: bacterial survivability is improved when said bacteria areencapsulated within fungal hosts. The bacterial endophyte (B from CE)SYM16660, when encompassed within a fungal host as part of the complexendophyte (CE) SYM16670 (SYM166), displays greater survivability ontreated corn seeds than does the isolated bacterial endophyte (B alone)SYM16660.

FIG. 5: bacterial endophyte tolerance to antibiotics is improved whensaid bacteria are encapsulated within fungal hosts. Samples were run on2% agarose gel. Endofungal bacterium EHB15779 16S remains detectable inits host fungus SYM15779 even after its host fungus is treated withgentamicin washes. Comparison treaments of SYM15779 not washed (presenceof both surface and endofungal bacteria) and washed (presence ofendofungal bacteria only) demonstrate presence of bacterial 16Ssequence. The non-complex endophyte SYM15890 spiked with a bacterialstrain and not washed with gentamicin shows a faint band of bacterial16S sequence, reflecting the presence of surface bacteria. Thenon-complex endophyte SYM15890 washed with gentamicin does not showpresence of bacterial 16S sequence.

DEFINITIONS

An “endophyteis an organism that lives within a plant or is otherwiseassociated therewith, and does not cause disease or harm the plantotherwise. Endophytes can occupy the intracellular or extracellularspaces of plant tissue, including the leaves, stems, flowers, fruits,seeds, or roots. An endophyte can be for example a bacterial or fungalorganism, and can confer a beneficial property to the host plant such asan increase in yield, biomass, resistance, or fitness. As used herein,the term “microbe” is sometimes used to describe an endophyte,particularly a fungal endophyte, that may be isolated from a fungalendophyte, and that may be capable of living within a plant.

The term “complex endophyte” is used to describe a host fungus thatencompasses at least one additional organism or composition, and thatcombination can itself be associated on or within a plant. Suchadditional organism or composition may be, for example, endofungalbacterial endophytes or endofungal fungal endophytes. As used herein, an“endophytic component” refers to an endofungal bacterial endophyte or anendofungal fungal endophyte.

“Endofungal bacterial endophyte” means a bacterial endophyte that iscapable of living inside a fungus, for example within the hyphae.Throughout this document, the term “endofungal bacterial endophyte” isused to denote bacterial endophytic entities originally isolated from ahost fungus or those that are capable of living within a host fungus.Likewise, “endofungal fungal endophyte” means a fungal endophyteoriginally isolated from a host fungus or one capable of living within ahost fungus In such cases, the term “endofungal” denotes either thesource of origin (host fungus) or capability of existing within a hostfungus, and is not meant to imply that the bacterium or fungus (orbacteria or fungi), is continually encompassed within a host fungus. Forexample, an endofungal bacterial endophyte may reside within a hostfungus for part of its life cycle and reside external to the host fungusfor other parts of its life cycle. In some cases, the term “componentbacterium” is used to denote a bacterium that exists within a hostfungus, or has been isolated from a host fungus.

In some embodiments, the host fungus comprises algae or cyanobacteria,or both, living in symbiosis (lichen), and at least one endofungalbacterial endophyte or endofungal fungal endophyte.

As used herein, the term “capable of” living inside a fungus means thatthe endophyte has the appropriate features permitting it to live insidea fungus. For example, the endophyte may produce the necessarysubstances to avoid rejection by the fungus, and be able to use thenutrients provided by the fungus to live.

As used herein, the term “bacterium” or “bacteria” refers in general toany prokaryotic organism, and may reference an organism from eitherKingdom Eubacteria (Bacteria), Kingdom Archaebacteria (Archae), or both.In some cases, bacterial genera have been reassigned due to variousreasons (such as but not limited to the evolving field of whole genomesequencing), and it is understood that such nomenclature reassignmentsare within the scope of any claimed genus. For example, certain speciesof the genus Erwinia have been described in the literature as belongingto genus Pantoea (Zhang and Qiu, 2015).

The term 16S refers to the DNA sequence of the 16S ribosomal RNA (rRNA)sequence of a bacterium. 16S rRNA gene sequencing is a well-establishedmethod for studying phylogeny and taxonomy of bacteria.

As used herein, the term “fungus” or “fungi” refers in general to anyorganism from Kingdom Fungi. Historical taxonomic classification offungi has been according to morphological presentation. Beginning in themid-1800's, it was became recognized that some fungi have a pleomorphiclife cycle, and that different nomenclature designations were being usedfor different forms of the same fungus. In 1981, the Sydney Congress ofthe International Mycological Association laid out rules for the namingof fungi according to their status as anamorph, teleomorph, or holomorph(Taylor, 2011). With the development of genomic sequencing, it becameevident that taxonomic classification based on molecular phylogeneticsdid not align with morphological-based nomenclature (Shenoy, 2007). As aresult, in 2011 the International Botanical Congress adopted aresolution approving the International Code of Nomenclature for Algae,Fungi, and Plants (Melbourne Code) (2012), with the stated outcome ofdesignating “One Fungus=One Name” (Hawksworth, 2012). However,systematics experts have not aligned on common nomenclature for allfungi, nor are all existing databases and information resourcesinclusive of updated taxonomies. As such, many fungi referenced hereinmay be described by their anamorph form but it is understood that basedon identical genomic sequencing, any pleomorphic state of that fungusmay be considered to be the same organism. For example, the genusAlternaria is the anamorph form of the teleomorph genus Lewia (Kwasna2003), ergo both would be understood to be the same organism with thesame DNA sequence. For example, it is understood that the genusAcremonium is also reported in the literature as genus Sarocladium aswell as genus Tilachilidium (Summerbell, 2011). For example, the genusCladosporium is an anamorph of the teleomorph genus Davidiella (Bensch,2012), and is understood to describe the same organism. In some cases,fungal genera have been reassigned due to various reasons, and it isunderstood that such nomenclature reassignments are within the scope ofany claimed genus. For example, certain species of the genusMicrodiplodia have been described in the literature as belonging togenus Paraconiothyrium (Crous and Groenveld, 2006).

“Internal Transcribed Spacer” (ITS) refers to the spacer DNA (non-codingDNA) situated between the small-subunit ribosomal RNA (rRNA) andlarge-subunit (LSU) rRNA genes in the chromosome or the correspondingtranscribed region in the polycistronic rRNA precursor transcript. ITSgene sequencing is a well-established method for studying phylogeny andtaxonomy of fungi. In some cases, the “Large SubUnit” (LSU) sequence isused to identify fungi. LSU gene sequencing is a well-established methodfor studying phylogeny and taxonomy of fungi. Some fungal endophytes ofthe present invention may be described by an ITS sequence and some maybe described by an LSU sequence. Both are understood to be equallydescriptive and accurate for determining taxonomy.

The terms “pathogen” and “pathogenic” in reference to a bacterium orfungus includes any such organism that is capable of causing oraffecting a disease, disorder or condition of a host comprising theorganism.

A “spore” or a population of “spores” refers to bacteria or fungi thatare generally viable, more resistant to environmental influences such asheat and bactericidal or fungicidal agents than other forms of the samebacteria or fungi, and typically capable of germination and out-growth.Bacteria and fungi that are “capable of forming spores” are thosebacteria and fungi comprising the genes and other necessary abilities toproduce spores under suitable environmental conditions.

“Biomass” means the total mass or weight (fresh or dry), at a giventime, of a plant tissue, plant tissues, an entire plant, or populationof plants. Biomass is usually given as weight per unit area. The termmay also refer to all the plants or species in the community (communitybiomass).

The term “isolated” is intended to specifically reference an organism,cell, tissue, polynucleotide, or polypeptide that is removed from itsoriginal source and purified from additional components with which itwas originally associated. For example, a complex endophyte may beconsidered isolated from a seed if it is removed from that seed sourceand purified so that it is isolated from any additional components withwhich it was originally associated. Similarly, a complex endophyte maybe removed and purified from a plant or plant element so that it isisolated and no longer associated with its source plant or plantelement. In some cases, the term “isolated” is used to describe abacterium of a complex endophyte that has been removed from its hostfungus

A “host plant” includes any plant, particularly a plant of agronomicimportance, which a complex endophyte can colonize. As used herein, anendophyte is said to “colonize” a plant or seed when it can be stablydetected within the plant or seed over a period time, such as one ormore days, weeks, months or years, in other words, a colonizing entityis not transiently associated with the plant or seed. In someembodiments, such host plants are plants of agronomic importance.

A “non-host target” means an organism or chemical compound that isaltered in some way after contacting a host plant or host fungus thatcomprises an endophyte, as a result of a property conferred to the hostplant or host fungus by the endophyte.

As used herein, a nucleic acid has “homology” or is “homologous” to asecond nucleic acid if the nucleic acid sequence has a similar sequenceto the second nucleic acid sequence. The terms “identity,” “percentsequence identity” or “identical” in the context of nucleic acidsequences refer to the residues in the two sequences that are the samewhen aligned for maximum correspondence. There are a number of differentalgorithms known in the art that can be used to measure nucleotidesequence identity. For instance, polynucleotide sequences can becompared using FASTA, Gap or Bestfit, which are programs in WisconsinPackage Version 10.0, Genetics Computer Group (GCG), Madison, Wis. FASTAprovides alignments and percent sequence identity of the regions of thebest overlap between the query and search sequences. (Pearson, 1990,Methods Enzymol. 183:63-98, incorporated herein by reference in itsentirety). The term “substantial homology” or “substantial similarity,”when referring to a nucleic acid or fragment thereof, indicates that,when optimally aligned with appropriate nucleotide insertions ordeletions with another nucleic acid (or its complementary strand), thereis nucleotide sequence identity in at least about 76%, 80%, 85%, or atleast about 90%, or at least about 95%, 96%, 97%, 98% 99%, 99.5% or 100%of the nucleotide bases, as measured by any well-known algorithm ofsequence identity, such as FASTA, BLAST or Gap, as discussed above. Insome embodiments, sequences can be compared using Geneious (Biomatters,Ltd., Auckland, New Zealand). In other embodiments, polynucleotidesequences can be compared using the multiple sequence alignmentalgorithm MUSCLE (Edgar RC, 2004).

As used herein, the terms “operational taxonomic unit,” “OTU,” “taxon,”“hierarchical cluster,” and “cluster” are used interchangeably. Anoperational taxon unit (OTU) refers to a group of one or more organismsthat comprises a node in a clustering tree. The level of a cluster isdetermined by its hierarchical order. In one embodiment, an OTU is agroup tentatively assumed to be a valid taxon for purposes ofphylogenetic analysis. In another embodiment, an OTU is any of theextant taxonomic units under study. In yet another embodiment, an OTU isgiven a name and a rank. For example, an OTU can represent a domain, asub-domain, a kingdom, a sub-kingdom, a phylum, a sub-phylum, a class, asub-class, an order, a sub-order, a family, a subfamily, a genus, asubgenus, or a species. In some embodiments, OTUs can represent one ormore organisms from the kingdoms eubacteria, protista, or fungi at anylevel of a hierarchal order. In some embodiments, an OTU represents aprokaryotic or fungal order.

In some embodiments, the invention uses endophytes that are heterologousto a plant element, for example in making synthetic combinations oragricultural formulations. A microbe is considered heterologous to theseed or plant if the seed or seedling that is unmodified (e.g., a seedor seedling that is not treated with an endophyte population describedherein) does not contain detectable levels of the microbe. For example,the invention contemplates the synthetic combinations of seeds orseedlings of agricultural plants and an endophytic microbe population(e.g., an isolated bacterium), in which the microbe population is“heterologously disposed” on the exterior surface of or within a tissueof the agricultural seed or seedling in an amount effective to colonizethe plant. A microbe is considered “heterologously disposed” on thesurface or within a plant (or tissue) when the microbe is applied ordisposed on the plant in a number that is not found on that plant beforeapplication of the microbe. For example, an endophyte population that isdisposed on an exterior surface or within the seed can be an endophyticbacterium that may be associated with the mature plant, but is not foundon the surface of or within the seed. As such, a microbe is deemedheterologously disposed when applied on the plant that either does notnaturally have the microbe on its surface or within the particulartissue to which the microbe is disposed, or does not naturally have themicrobe on its surface or within the particular tissue in the numberthat is being applied. In another example, an endophyte that is normallyassociated with leaf tissue of a cupressaceous tree sample would beconsidered heterologous to leaf tissue of a maize plant. In anotherexample, an endophyte that is normally associated with leaf tissue of amaize plant is considered heterologous to a leaf tissue of another maizeplant that naturally lacks said endophyte. In another example, a complexendophyte that is normally associated at low levels in a plant isconsidered heterologous to that plant if a higher concentration of thatendophyte is introduced into the plant.

In some embodiments, a microbe can be “endogenous” to a seed or plant,or a bacterium may be “endogenous” to a fungal host with which it formsa complex endophyte. As used herein, a microbe is considered“endogenous” to a plant or seed, if the endophyte or endophyte componentis derived from, or is otherwise found in, a plant element of the plantspecimen from which it is sourced. Further, an endophyte is considered“endogenous” to a fungal host, if the endophyte is derived from, or isotherwise found in, a fungal host. For example, a complex endophyte maybe isolated and purified, said complex endophyte comprising a hostfungus and an endogenous bacterium.

The term “isoline” is a comparative term, and references organisms thatare genetically identical, but may differ in treatment. In one example,two genetically identical maize plant embryos may be separated into twodifferent groups, one receiving a treatment (such as transformation witha heterologous polynucleotide, to create a genetically modified plant)and one control that does not receive such treatment. Any phenotypicdifferences between the two groups may thus be attributed solely to thetreatment and not to any inherency of the plant's genetic makeup. Inanother example, two genetically identical soybean seeds may be treatedwith a formulation that introduces an endophyte composition. Anyphenotypic differences between the plants grown from those seeds may beattributed to the treatment, thus forming an isoline comparison.

Similarly, by the term “reference agricultural plant”, it is meant anagricultural plant of the same species, strain, or cultivar to which atreatment, formulation, composition or endophyte preparation asdescribed herein is not administered/contacted. A reference agriculturalplant, therefore, is identical to the treated plant with the exceptionof the presence of the endophyte and can serve as a control fordetecting the effects of the endophyte that is conferred to the plant.

A “reference environment” refers to the environment, treatment orcondition of the plant in which a measurement is made. For example,production of a compound in a plant associated with an endophyte can bemeasured in a reference environment of drought stress, and compared withthe levels of the compound in a reference agricultural plant under thesame conditions of drought stress. Alternatively, the levels of acompound in plant associated with an endophyte and referenceagricultural plant can be measured under identical conditions of nostress.

A “plant element” is intended to generically reference either a wholeplant or a plant component, including but not limited to plant tissues,parts, and cell types. A plant element may be one of the following:whole plant, seedling, meristematic tissue, ground tissue, vasculartissue, dermal tissue, seed, leaf, root, shoot, stem, flower, fruit,stolon, bulb, tuber, corm, kelkis, shoot, bud. As used herein, a “plantelement” is synonymous to a “portion” of a plant, and refers to any partof the plant, and can include distinct tissues and/or organs, and may beused interchangeably with the term “tissue” throughout.

Similarly, a “plant reproductive element” is intended to genericallyreference any part of a plant that is able to initiate other plants viaeither sexual or asexual reproduction of that plant, for example but notlimited to: seed, seedling, root, shoot, stolon, bulb, tuber, corm,keikis, or bud.

A “progeny seed”, as used herein, refers to the seed produced by a hostplant that has been inoculated with, or associated with, an endophyte.For example, in the present invention, a seed, plant element, or wholeplant may become heterologously associated with an endophyte, and theplant that is grown from said seed, or plant that is grown inheterologous association with said endophyte, may itself produce progenyseeds that comprise altered nutritional composition compared to seedsobtained from plants that were not grown from a plant element associatedwith an endophyte or obtained from a parental (host) plant that hadbecome associated with an endophyte at some point in its life cycle. Inthe general sense, the phrase “progeny seed” may be construed torepresent any plant propagative unit produced by the host plant that iscapable of becoming another individual of that same plant species.

A “population” of plants, as used herein, can refer to a plurality ofplants that were subjected to the same inoculation methods describedherein, or a plurality of plants that are progeny of a plant or group ofplants that were subjected to the inoculation methods. In addition, apopulation of plants can be a group of plants that are grown from coatedseeds. The plants within a population will typically be of the samespecies, and will also typically share a common genetic derivation.

As used herein, an “agricultural seed” is a seed used to grow a planttypically used in agriculture (an “agricultural plant”). The seed may beof a monocot or dicot plant, and may be planted for the production of anagricultural product, for example feed, food, fiber, fuel, etc. As usedherein, an agricultural seed is a seed that is prepared for planting,for example, in farms for growing.

The term “synthetic combination” means a plurality of elementsassociated by human endeavor, in which said association is not found innature. In the present invention, “synthetic combination” is used torefer to a treatment formulation associated with a plant element.

A “treatment formulation” refers to a mixture of chemicals thatfacilitate the stability, storage, and/or application of the endophytecomposition(s). In some embodiments, an agriculturally compatiblecarrier can be used to formulate an agricultural formulation or othercomposition that includes a purified endophyte preparation. As usedherein an “agriculturally compatible carrier” refers to any material,other than water, that can be added to a plant element without causingor having an adverse effect on the plant element (e.g., reducing seedgermination) or the plant that grows from the plant element, or thelike.

The compositions and methods herein may provide for an improved“agronomic trait” or “trait of agronomic importance” to a host plant,which may include, but not be limited to, the following: diseaseresistance, drought tolerance, heat tolerance, cold tolerance, salinitytolerance, metal tolerance, herbicide tolerance, improved water useefficiency, improved nitrogen utilization, improved nitrogen fixation,pest resistance, herbivore resistance, pathogen resistance, yieldimprovement, health enhancement, vigor improvement, growth improvement,photosynthetic capability improvement, nutrition enhancement, alteredprotein content, altered oil content, increased biomass, increased shootlength, increased root length, improved root architecture, modulation ofa metabolite, modulation of the proteome, increased seed weight, alteredseed carbohydrate composition, altered seed oil composition, alteredseed protein composition, altered seed nutritional quality trait,compared to an isoline plant grown from a seed without said seedtreatment formulation.

The phrase “nutritional quality trait” includes any measureableparameter of a seed that either directly or indirectly influences thevalue (nutritional or economic) of said seed, for example, but notlimited to: protein, fat, carbohydrate, ash, moisture, fiber, andCalories. In some cases, “nutritional quality trait” is synonymous with“nutritional quality trait” or “seed nutritional quality trait”, and canrefer to any composition of the associated plant element, mostparticularly compositions providing benefit to other organisms thatconsume or utilize said plant element.

As used herein, the terms “water-limited (or water-limiting) condition”and “drought condition”, or “water-limited” and “drought”, or “waterstress” and “drought stress”, may all be used interchangeably. Forexample, a method or composition for improving a plant's ability togrown under drought conditions means the same as the ability to growunder water-limited conditions. In such cases, the plant can be furthersaid to display improved drought tolerance.

Additionally, “altered metabolic function” or “altered enzymaticfunction” may include, but not be limited to, the following: alteredproduction of an auxin, altered nitrogen fixation, altered production ofan antimicrobial compound, altered production of a siderophore, alteredmineral phosphate solubilization, altered production of a cellulase,altered production of a chitinase, altered production of a xylanase,altered production of acetoin.

An “increased yield” can refer to any increase in biomass or seed orfruit weight, seed size, seed number per plant, seed number per unitarea, bushels per acre, tons per acre, kilo per hectare, or carbohydrateyield. Typically, the particular characteristic is designated whenreferring to increased yield, e.g., increased grain yield or increasedseed size.

In some cases, the present invention contemplates the use ofcompositions that are “compatible” with agricultural chemicals, forexample, a fungicide, an anti-complex compound, or any other agentwidely used in agricultural which has the effect of killing or otherwiseinterfering with optimal growth of another organism. As used herein, acomposition is “compatible” with an agricultural chemical when theorganism is modified, such as by genetic modification, e.g., contains atransgene that confers resistance to an herbicide, or is adapted to growin, or otherwise survive, the concentration of the agricultural chemicalused in agriculture. For example, an endophyte disposed on the surfaceof a seed is compatible with the fungicide metalaxyl if it is able tosurvive the concentrations that are applied on the seed surface.

As used herein, a “colony-forming unit” (“CFU”) is used as a measure ofviable microorganisms in a sample. A CFU is an individual viable cellcapable of forming on a solid medium a visible colony whose individualcells are derived by cell division from one parental cell.

The term “efficacy” (and its synonyms, such as “efficacious”) as usedherein describes the capability of a microbe to perform its function. Inone non-limiting example, a complex endophyte is said to be efficaciousif it is capable of performing a function such as improving the yield ofa plant with which it becomes associated. In another non-limitingexample, a bacterial endophyte is said to display improved efficacy ifit is capable of performing a particular function under one conditionvs. a control condition.

The terms “decreased”, “fewer”, “slower” and “increased” “faster”“enhanced” “greater” as used herein refers to a decrease or increase ina characteristic of the endophyte treated seed or resulting plantcompared to an untreated seed or resulting plant. For example, adecrease in a characteristic may be at least 1%, between 1% and 2%, atleast 2%, between 2% and 3%, at least 3%, between 3% and 4%, at least4%, between 4% and 5%, at least 5%, between 5% and 10%, at least 10%,between 10% and 15%, at least 15%, between 15% and 20%, at least 20%,between 20% and 25%, at least 25%, between 25% and 30%, at least 30%,between 30% and 35%, at least 35%, between 35% and 40%, at least 40%,between 40% and 45%, at least 45%, between 45% and 50%, at least 50%,between 50% and 60%, at least about 60%, between 60% and 75%, at least75%, between 75% and 80%, at least about 80%, between 80% and 90%, atleast about 90%, between 90% and 100%, at least 100%, between 100% and200%, at least 200%, between 200% and 300%, at least about 300%, between300% and 400%, at least about 400% or more lower than the untreatedcontrol, and an increase may be at least 1%, between 1% and 2%, at least2%, between 2% and 3%, at least 3%, between 3% and 4%, at least 4%,between 4% and 5%, at least 5%, between 5% and 10%, at least 10%,between 10% and 15%, at least 15%, between 15% and 20%, at least 20%,between 20% and 25%, at least 25%, between 25% and 30%, at least 30%,between 30% and 35%, at least 35%, between 35% and 40%, at least 40%,between 40% and 45%, at least 45%, between 45% and 50%, at least 50%,between 50% and 60%, at least about 60%, between 60% and 75%, at least75%, between 75% and 80%, at least about 80%, between 80% and 90%, atleast about 90%, between 90% and 100%, at least 100%, between 100% and200%, at least 200%, between 200% and 300%, at least about 300%, between300% and 400%, at least about 400% or more higher than the untreatedcontrol.

DETAILED DESCRIPTION OF THE INVENTION

As demonstrated herein, agricultural plants associate with symbioticmicroorganisms termed endophytes, particularly bacteria and fungi, whichmay contribute to plant survival and performance. However, modernagricultural processes may have perturbed this relationship, resultingin increased crop losses, diminished stress resilience, biodiversitylosses, and increasing dependence on external chemicals, fertilizers,and other unsustainable agricultural practices. There is a need fornovel methods for generating plants with novel microbiome propertiesthat can sustainably increase yield, stress resilience, and decreasefertilizer and chemical use.

Currently, the generally accepted view of plant endophytic communitiesfocuses on their homologous derivation, predominantly from the soilcommunities in which the plants are grown (Hallman et al., (1997)Canadian Journal of Microbiology. 43(10): 895-914). Upon observingtaxonomic overlap between the endophytic and soil microbiota in A.thaliana, it was stated, “Our rigorous definition of an endophyticcompartment microbiome should facilitate controlled dissection ofplant-microbe interactions derived from complex soil communities”(Lundberg et al., (2012) Nature. 488, 86-90). There is strong support inthe art for soil representing the repository from which plant endophytesare derived (Long et al., 2010, New Phytologist 185: 554-567,incorporated herein by reference in its entirety). Notable plant-microbeinteractions such as mycorrhyzal fungi and complex rhizobia fit theparadigm of soil-based colonization of plant hosts and appear toprimarily establish themselves independently. As a result of focusingattention on the derivation of endophytes from the soil in which thetarget agricultural plant is currently growing, there has been aninability to achieve commercially significant improvements in plantyields and other plant characteristics such as increased root biomass,increased root length, increased height, increased shoot length,increased leaf number, increased water use efficiency, increased overallbiomass, increase grain yield, increased photosynthesis rate, increasedtolerance to drought, increased heat tolerance, increased salttolerance, increased resistance to insect and nematode stresses,increased resistance to a fungal pathogen, increased resistance to acomplex pathogen, increased resistance to a viral pathogen, a detectablemodulation in the level of a metabolite, and a detectable modulation inthe proteome relative to a reference plant.

Complex endophytes, or endophytes that themselves further comprise anadditional organism or composition, are rarely described. Because of thelack of evidence in the literature for both the existence of complexendophytes in crop plant populations, as well as the lack of evidencedemonstrating any benefit to the host plant conferred from an endophyte,complex endophytes have not previously been conceived as a viablemechanism to address the need to provide improved yield and tolerance toenvironmental stresses for plants of agricultural importance.

The inventors herein have conceived of utilizing complex endophytecompositions or compositions comprising endophytic components for use inbenefitting plant health and stress tolerance, as well as methods ofusing said complex endophyte compositions or compositions comprisingendophytic components, to impart novel characteristics to a host fungusor a host plant. In one aspect of this invention, endophyte compositionsare isolated and purified from plant sources, and synthetically combinedwith a plant element, such as a seed, to impart improved agronomicpotential and/or improved agronomic traits to the host plant. In anotheraspect of the invention, endophytic components, such as endofungalbacteria or endofungal fungi, are isolated and purified from theirnative source(s) and synthetically combined with a plant element, toimpart improved agronomic potential and/or improved agronomic traits tothe host plant. Such endofungal components may be further manipulated orcombined with additional elements prior to combining with the plantelement(s).

The aspects of the present invention are surprising for a number ofreasons. First, crop plants have not been shown to comprise complexendophytes, and even for the few plants in which complex endophytes havebeen found, no benefit has been described. Secondly, complexendophyte-host associations are hypothesized in the literature to nothave evolved for the manifestation of any particular phenotype of thehost plant. Rather, the association seems to be driven by an accident ofco-localization in the same geographical region.

As described herein, beneficial organisms can be robustly derived fromheterologous, endogenous, or engineered sources, optionally cultured,administered heterologously to plant elements, and, as a result of theadministration, confer multiple beneficial properties. This issurprising given the variability observed in the art in endophyticmicrobe isolation and the previous observations of inefficient seedpathogen colonization of plant host's tissues. Further, the ability ofheterologously disposed complex endophytes to colonize plantreproductive elements from the outside is surprising, given thatisolated complex endophytes have not been previously demonstrated to becapable of penetrating and colonizing host tissues.

In part, the present invention describes preparations of complexendophytes, and the creation of synthetic combinations of seeds and/orseedlings with heterologous complex endophyte compositions, andformulations containing the synthetic combinations, as well as therecognition that such synthetic combinations display a diversity ofbeneficial properties in the agricultural plants. Such beneficialproperties include metabolism, transcript expression, proteomealterations, morphology, and the resilience to a variety ofenvironmental stresses, and the combination of a plurality of suchproperties. The present invention also describes methods of using suchcomplex endophyte compositions to benefit the host plant with which itis associated.

Isolated Complex Endophyte Compositions and Methods

The isolated complex endophytes described herein provide several keysignificant advantages over other plant-associated microbes. Differentenvironments can contain significantly different populations ofendophytes and thus may provide reservoirs for desired complexendophytes and/or components (such as endofungal bacterial endophytes orendofungal fungal endophytes). Once a choice environment is selected,plant elements of choice plants to be sampled can be identified by theirhealthy and/or robust growth, or other desired phenotypiccharacteristics.

In one aspect of the present invention, the complex endophytes usefulfor the present invention can also be isolated from plants or plantelements adapted to a particular environment, including, but not limitedto, an environment with water deficiency, salinity, acute and/or chronicheat stress, acute and/or chronic cold stress, nutrient deprived soilsincluding, but not limited to, micronutrient deprived soils,macronutrient (e.g., potassium, phosphate, nitrogen) deprived soils,pathogen stress, including fungal, nematode, insect, viral, complexpathogen stress.

In one embodiment, a plant comprising a complex endophyte is harvestedfrom a soil type different than that in which the plant is normallygrown. In another embodiment, the plant comprising a complex endophyteis harvested from an ecosystem where the agricultural plant is notnormally found. In another embodiment, the plant comprising a complexendophyte is harvested from a soil with an average pH range that isdifferent from the optimal soil pH range of the agricultural plant. Inone embodiment, the plant comprising a complex endophyte is harvestedfrom an environment with average air temperatures lower than the normalgrowing temperature of the agricultural plant. In one embodiment, theplant comprising a complex endophyte is harvested from an environmentwith average air temperatures higher than the normal growing temperatureof the agricultural plant. In another embodiment, the plant comprising acomplex endophyte is harvested from an environment with average rainfalllower than the optimal average rainfall received by the agriculturalplant. In one embodiment, the plant comprising a complex endophyte isharvested from an environment with average rainfall higher than theoptimal average rainfall of the agricultural plant. In anotherembodiment, the plant comprising a complex endophyte is harvested from asoil type with different soil moisture classification than the normalsoil type that the agricultural plant is grown on. In one embodiment,the plant comprising a complex endophyte is harvested from anenvironment with average rainfall lower than the optimal averagerainfall of the agricultural plant. In one embodiment, the plantcomprising a complex endophyte is harvested from an environment withaverage rainfall higher than the optimal average rainfall of theagricultural plant. In another embodiment, the plant comprising acomplex endophyte is harvested from an agricultural environment with ayield lower than the average yield expected from the agricultural plantgrown under average cultivation practices on normal agricultural land.In another embodiment, the plant comprising a complex endophyte isharvested from an agricultural environment with a yield lower than theaverage yield expected from the agricultural plant grown under averagecultivation practices on normal agricultural land. In anotherembodiment, the plant comprising a complex endophyte is harvested froman environment with average yield higher than the optimal average yieldof the agricultural plant. In another embodiment, the plant comprising acomplex endophyte is harvested from an environment with average yieldhigher than the optimal average yield of the agricultural plant. Inanother embodiment, the plant comprising a complex endophyte isharvested from an environment where soil contains lower total nitrogenthan the optimum levels recommended in order to achieve average yieldsfor a plant grown under average cultivation practices on normalagricultural land. In another embodiment, the plant comprising a complexendophyte is harvested from an environment where soil contains highertotal nitrogen than the optimum levels recommended in order to achieveaverage yields for a plant grown under average cultivation practices onnormal agricultural land. In another embodiment, the plant comprising acomplex endophyte is harvested from an environment where soil containslower total phosphorus than the optimum levels recommended in order toachieve average yields for a plant grown under average cultivationpractices on normal agricultural land. In another embodiment, the plantcomprising a complex endophyte is harvested from an environment wheresoil contains higher total phosphorus than the optimum levelsrecommended in order to achieve average yields for a plant grown underaverage cultivation practices on normal agricultural land. In anotherembodiment, the plant comprising a complex endophyte is harvested froman environment where soil contains lower total potassium than theoptimum levels recommended in order to achieve average yields for aplant grown under average cultivation practices on normal agriculturalland. In another embodiment, the plant comprising a complex endophyte isharvested from an environment where soil contains higher total potassiumthan the optimum levels recommended in order to achieve average yieldsfor a plant grown under average cultivation practices on normalagricultural land. In another embodiment, the plant comprising a complexendophyte is harvested from an environment where soil contains lowertotal sulfur than the optimum levels recommended in order to achieveaverage yields for a plant grown under average cultivation practices onnormal agricultural land. In another embodiment, the plant comprising acomplex endophyte is harvested from an environment where soil containshigher total sulfur than the optimum levels recommended in order toachieve average yields for a plant grown under average cultivationpractices on normal agricultural land. In another embodiment, the plantcomprising a complex endophyte is harvested from an environment wheresoil contains lower total calcium than the optimum levels recommended inorder to achieve average yields for a plant grown under averagecultivation practices on normal agricultural land. In anotherembodiment, the plant comprising a complex endophyte is harvested froman environment where soil contains lower total magnesium than theoptimum levels recommended in order to achieve average yields for aplant grown under average cultivation practices on normal agriculturalland. In another embodiment, the plant comprising a complex endophyte isharvested from an environment where soil contains higher total sodiumchloride (salt) than the optimum levels recommended in order to achieveaverage yields for a plant grown under average cultivation practices onnormal agricultural land.

In some embodiments, this invention relates to purified isolated complexendophytes from, for example, maize, wheat, rice, barley, soybeans,cotton, canola, tomatoes, or other agricultural plants, and compositionssuch as agricultural formulations or articles of manufacture thatinclude such purified populations, as well as methods of using suchpopulations to make synthetic combinations or agricultural products.

In some embodiments, this invention relates to the usage of a fungus asa carrier of an endophyte, and methods of using said fungus. In suchcases, the fungus can act as a protective mechanism for an endophyte,such as a bacterium or another fungus, that otherwise has lowsurvivability in a formulation. Gram-negative bacteria, for example, donot survive well when used to treat plant elements. It may therefore bedesirable to identify a complex endophyte comprising a componentendofungal bacterium or fungus that is identical to or similar to abacterium or fungus that provides a benefit to a plant, and introducesuch complex endophyte to a plant element in such a manner that thebeneficial endophytic bacterium or fungus is protected from desiccation,mechanical trauma, or chemical exposure. In another embodiment, thisinvention relates to the usage of a fungus to deploy a non-spore formingbacterium or fungus. It may be desirable to identify a spore-formingcomplex endophyte comprising a component endofungal bacteria or fungusthat is identical to or similar to a non-spore-forming bacterium orfungus that provides a benefit to a plant. Therefore, one aspect of thisinvention is a fungus that acts as an endophytic carrier to enabledeployment of beneficial bacteria or fungi that could otherwise not beturned into a product.

It is also contemplated that a lichen or lichenized fungus could a hostorganism in an endophytic complex. The lichen-associated bacteria,cyanobacteria, and/or fungus can be used as endophytes, either as acomplex or individually.

Isolated complex endophytes or components thereof, used to make asynthetic composition can be obtained from a plant element of manydistinct plants. In one embodiment, the complex endophyte can beobtained a plant element of the same or different crop, and can be fromthe same or different cultivar or variety as the plant element to whichthe composition is intended to be association.

In another embodiment, isolated complex endophytes or componentsthereof, used to make a synthetic composition can be obtained from thesame cultivar or species of agricultural plant to which the compositionis intended for association, or can be obtained from a differentcultivar or species of agricultural plant. For example, complexendophytes from a particular corn variety can be isolated and coatedonto the surface of a corn seed of the same variety.

In another embodiment, isolated complex endophytes or componentsthereof, used to make a synthetic composition can be obtained from aplant element of a plant that is related to the plant element to whichthe composition is intended to be association. For example, an endophyteisolated from Triticum monococcum (einkorn wheat) can be coated onto thesurface of a T. aestivum (common wheat) seed; or, an endophyte fromHordeum vulgare (barley) can be isolated and coated onto the seed of amember of the Triticeae family, for example, seeds of the rye plant,Secale cereale).

In still another embodiment, isolated complex endophytes or componentsthereof, used to make a synthetic composition can be obtained from aplant element of a plant that is distantly related to the seed ontowhich the endophyte is to be coated. For example, a tomato-derivedendophyte can be isolated and coated onto a rice seed.

In some embodiments, a synthetic combination is used that includes twoor more (e.g., 3, 4, 5, 6, 7, 8, 9, 10, between 10 and 15, 15, between15 and 20, 20, between 20 and 25, 25, or greater than 25) differentcomplex endophytes, e.g., obtained from different families or differentgenera, or from the same genera but different species. The differentcomplex endophytes can be obtained from the same cultivar ofagricultural plant (e.g., the same maize, wheat, rice, or barley plant),different cultivars of the same agricultural plant (e.g., two or morecultivars of maize, two or more cultivars of wheat, two or morecultivars of rice, or two or more cultivars of barley), or differentspecies of the same type of agricultural plant (e.g., two or moredifferent species of maize, two or more different species of wheat, twoor more different species of rice, or two or more different species ofbarley). In embodiments in which two or more complex endophytes areused, each of the endophytes can have different properties oractivities, e.g., produce different metabolites, produce differentenzymes such as different hydrolytic enzymes, confer differentbeneficial traits, or colonize different elements of a plant (e.g.,leaves, stems, flowers, fruits, seeds, or roots). For example, oneendophyte can colonize a first tissue and a second endophyte cancolonize a tissue that differs from the first tissue. Combinations ofendophytes are disclosed in detail below.

In one embodiment, the complex endophyte is isolated from a differentplant than the inoculated plant. For example, in one embodiment, theendophyte is an endophyte isolated from a different plant of the samespecies as the inoculated plant. In some cases, the endophyte isisolated from a species related to the inoculated plant.

In some embodiments, the complex endophyte comprises an endofungalfungal endophyte of one or more of the following taxa: Alternaria,Aureobasidium, Biscogniauxia, Botryosphaeria, Cladosporium,Coniothyrium, Daldinia, Fusarium, Hormonema, Hypoxylon, Lecythophora,Microdiplodia, Monodictys, Nectria, Neurospora, Paraconiothyrium,Penicillium, Periconia, Pestalotiopsis, Phaeomoniella, Phoma,Phyllosticta, Preussia, Xylaria, Rhizopus, Aspergillus, Gigaspora,Piriformospora, Laccaria, Tuber, Mucor.

In some embodiments, the complex endophyte comprises a host funguschosen among those listed in Table 2, or those comprising a fungal ITSor LSU nucleic acid sequence that is at least 97% identical to at leastone of the ITS or LSU nucleic acid sequences of the fungi listed inTable 2 (SEQ ID NOs: 250-333).

In some embodiments, the complex endophyte comprises a host fungus fromthe genus Botryosphaeria. In some embodiments, the complex endophytecomprises a host fungus that itself comprises an ITS nucleic acidsequence that is at least 97% identical to SEQ ID NO: 266. In someembodiments, the complex endophyte comprises a host fungus that itselfcomprises an ITS nucleic acid sequence that is at least 97% identical toSEQ ID NO: 325.

In some embodiments, the complex endophyte comprises a host fungus fromthe genus Mucor. In some embodiments, the complex endophyte comprises ahost fungus that itself comprises an ITS nucleic acid sequence that isat least 97% identical to SEQ ID NO: 333.

In some embodiments, the complex endophyte comprises a host fungus fromthe genus Microdiplodia (also known variously as Paraconiothyrium). Insome embodiments, the complex endophyte comprises a host fungus thatitself comprises an ITS nucleic acid sequence that is at least 97%identical to SEQ ID NO: 268. In some embodiments, the complex endophytecomprises a host fungus that itself comprises an ITS nucleic acidsequence that is at least 97% identical to SEQ ID NO: 270. In someembodiments, the complex endophyte comprises a host fungus that itselfcomprises an ITS nucleic acid sequence that is at least 97% identical toSEQ ID NO: 326. In some embodiments, the complex endophyte comprises ahost fungus that itself comprises an ITS nucleic acid sequence that isat least 97% identical to SEQ ID NO: 331.

In some embodiments, the complex endophyte comprises a host fungus fromthe genus Pestalotiposis. In some embodiments, the complex endophytecomprises a host fungus that itself comprises an ITS nucleic acidsequence that is at least 97% identical to SEQ ID NO: 269. In someembodiments, the complex endophyte comprises a host fungus that itselfcomprises an ITS nucleic acid sequence that is at least 97% identical toSEQ ID NO: 327.

In some embodiments, the complex endophyte comprises a host fungus fromthe genus Phyllosticta. In some embodiments, the complex endophytecomprises a host fungus that itself comprises an ITS nucleic acidsequence that is at least 97% identical to SEQ ID NO: 267. In someembodiments, the complex endophyte comprises a host fungus that itselfcomprises an ITS nucleic acid sequence that is at least 97% identical toSEQ ID NO: 328.

In some embodiments, the complex endophyte comprises a host fungus fromthe genus Alternaria. In some embodiments, the complex endophytecomprises a host fungus that itself comprises an LSU nucleic acidsequence that is at least 97% identical to SEQ ID NO: 329.

In some embodiments, the complex endophyte comprises a host fungus fromthe genus Lecythophora. In some embodiments, the complex endophytecomprises a host fungus that itself comprises an ITS nucleic acidsequence that is at least 97% identical to SEQ ID NO: 247. In someembodiments, the complex endophyte comprises a host fungus that itselfcomprises an ITS nucleic acid sequence that is at least 97% identical toSEQ ID NO: 330.

In some embodiments, the complex endophyte comprises a host fungus fromthe genus Daldinia. In some embodiments, the complex endophyte comprisesa host fungus that itself comprises an ITS nucleic acid sequence that isat least 97% identical to SEQ ID NO: 242. In some embodiments, thecomplex endophyte comprises a host fungus that itself comprises an ITSnucleic acid sequence that is at least 97% identical to SEQ ID NO: 260.In some embodiments, the complex endophyte comprises a host fungus thatitself comprises an ITS nucleic acid sequence that is at least 97%identical to SEQ ID NO: 263. In some embodiments, the complex endophytecomprises a host fungus that itself comprises an ITS nucleic acidsequence that is at least 97% identical to SEQ ID NO: 332.

In some embodiments, the complex endophyte comprises an endofungalfungal endophyte of one or more of the following taxa: Alternaria,Aureobasidium, Biscogniauxia, Botryosphaeria, Cladosporium,Coniothyrium, Daldinia, Fusarium, Hormonema, Hypoxylon, Lecythophora,Microdiplodia, Monodictys, Nectria, Neurospora, Paraconiothyrium,Pestalotiopsis, Phaeomoniella, Phoma, Phyllosticta, Preussia, Xylaria,Rhizopus, Aspergillus, Gigaspora, Piriformospora, Laccaria, Tuber,Mucor.

In some embodiments, the complex endophyte comprises an endofungalfungal endophyte chosen among those listed in Table 2, or thosecomprising a fungal ITS or LSU nucleic acid sequence that is at least97% identical to at least one of the ITS or LSU nucleic acid sequencesof the fungi listed in Table 2 (SEQ ID NOs: 250-333).

In some embodiments of the present invention, the complex endophytecomprises a bacterium.

In some embodiments of the present invention, the complex endophytecomprises an endofungal bacterial endophyte of one or more of thefollowing taxa: Acinetobacter, Actinoplanes, Adlercreutzia, Afipia,Atopostipes, Bacillus, Beijerinckia, Bradyrhizobium, Burkholderia,Candidatus Haloredivivus, Caulobacter, Chryseobacterium,Coraliomargarita, Curtobacterium, Delftia, Dyella, Enhydrobacter,Enterobacter, Erwinia, Escherichia/Shigella, Exiguobacterium,Ferroglobus, Filimonas, Halobaculum, Halosimplex, Herbaspirillum,Hymenobacter, Kosakonia, Lactobacillus, Luteibacter, Massilia,Mesorhizobium, Microbacterium, Okibacterium, Oligotropha, Oryzihumus,Paenibacillus, Pantoea, Pelomonas, Perlucidibaca, Polynucleobacter,Propionibacterium, Pseudoclavibacter, Pseudomonas, Ralstonia, Rhizobium,Rhodococcus, Rhodopseudomonas, Sebaldella, Serratia, Sinosporangium,Sphingomonas, Staphylococcus, Stenotrophomonas, Streptococcus,Stygiolobus, Sulfurisphaera, Variovorax, WPS-2_genera_incertae_sedis,Zimmermannella, Burkholderia, Streptomyces, Candidatus, Rhizobium,Paenibacillus.

In some embodiments, the complex endophyte comprises an endofungalbacterial endophyte chosen among those listed in Table 1, or thosecomprising a 16S nucleic acid sequence that is at least 97% identical toat least one of the 16S nucleic acid sequence of the bacteria listed inTable 1 (SEQ ID NOs: 1-249).

In some embodiments, the complex endophyte comprises a componentbacterium from the genus Luteibacter. In some embodiments, the complexendophyte comprises a component bacterium from the genus Dyella.

In some embodiments, the complex endophyte comprises a host fungus thatitself comprises a 16S nucleic acid sequence that is at least 97%identical to SEQ ID NO 45. In some embodiments, the complex endophytecomprises a host fungus that itself comprises a 16S nucleic acidsequence that is at least 97% identical to SEQ ID NO 48. In someembodiments, the complex endophyte comprises a host fungus that itselfcomprises a 16S nucleic acid sequence that is at least 97% identical toSEQ ID NO 237. In some embodiments, the complex endophyte comprises ahost fungus that itself comprises a 16S nucleic acid sequence that is atleast 97% identical to SEQ ID NO 240.

In some embodiments, the complex endophyte comprises a componentbacterium from the genus Pantoea. In some embodiments, the complexendophyte comprises a host fungus that itself comprises a 16S nucleicacid sequence that is at least 97% identical to SEQ ID NO: 55. In someembodiments, the complex endophyte comprises a host fungus that itselfcomprises a 16S nucleic acid sequence that is at least 97% identical toSEQ ID NO: 238. In some embodiments, the complex endophyte comprises ahost fungus that itself comprises a 16S nucleic acid sequence that is atleast 97% identical to SEQ ID NO: 249.

In some embodiments, the complex endophyte comprises a componentbacterium from the genus Luteibacter. In some embodiments, the complexendophyte comprises a host fungus that itself comprises a 16S nucleicacid sequence that is at least 97% identical to SEQ ID NO: 9. In someembodiments, the complex endophyte comprises a host fungus that itselfcomprises a 16S nucleic acid sequence that is at least 97% identical toSEQ ID NO: 31. In some embodiments, the complex endophyte comprises ahost fungus that itself comprises a 16S nucleic acid sequence that is atleast 97% identical to SEQ ID NO: 40. In some embodiments, the complexendophyte comprises a host fungus that itself comprises a 16S nucleicacid sequence that is at least 97% identical to SEQ ID NO: 58. In someembodiments, the complex endophyte comprises a host fungus that itselfcomprises a 16S nucleic acid sequence that is at least 97% identical toSEQ ID NO: 239. In some embodiments, the complex endophyte comprises ahost fungus that itself comprises a 16S nucleic acid sequence that is atleast 97% identical to SEQ ID NO: 241.

In some embodiments, the complex endophyte comprises a componentbacterium from the genus Ralstonia. In some embodiments, the complexendophyte comprises a host fungus that itself comprises a 16S nucleicacid sequence that is at least 97% identical to SEQ ID NO: 16. In someembodiments, the complex endophyte comprises a host fungus that itselfcomprises a 16S nucleic acid sequence that is at least 97% identical toSEQ ID NO: 242.

In some embodiments, the complex endophyte comprises a componentbacterium from the genus Erwinia. In some embodiments, the complexendophyte comprises a host fungus that itself comprises a 16S nucleicacid sequence that is at least 97% identical to SEQ ID NO: 62. In someembodiments, the complex endophyte comprises a host fungus that itselfcomprises a 16S nucleic acid sequence that is at least 97% identical toSEQ ID NO: 243.

In some embodiments, the complex endophyte comprises a componentbacterium from the genus Bacillus. In some embodiments, the complexendophyte comprises a host fungus that itself comprises a 16S nucleicacid sequence that is at least 97% identical to SEQ ID NO: 50. In someembodiments, the complex endophyte comprises a host fungus that itselfcomprises a 16S nucleic acid sequence that is at least 97% identical toSEQ ID NO: 244.

The isolated complex endophytes of the present invention mayindividually comprise single additional components (for example, a hostfungus may comprise a single endofungal bacterial endophyte), aplurality of components of the same type (for example, a host fungus maycomprise multiple endofungal bacterial endophytes of different strains),or a plurality of components of different types (for example, a hostfungus may comprise multiple endofungal bacterial endophytes ofdifferent strains; in another example, a host fungus may comprise bothendofungal bacterial endophytes and endofungal fungal endophytes).

In other embodiments, the complex endophyte is selected from one of thecomplex endophytes described in Table 3 or Table 4.

In some aspects of the present invention, the complex endophyte,comprising a host fungus and a component bacterium, may be selected fromthe combination of host fungi and component bacteria represented by thefollowing SEQ ID combinations. For example, a complex endophyte may be acombination of a Bacterium comprising a nucleotide sequence at least 97%identical to SEQ ID NO: 237 and a Fungus comprising a nucleotidesequence at least 97% identical to SEQ ID NO: 325. In another example, acomplex endophyte may be a combination of a Bacterium comprising anucleotide sequence at least 97% identical to SEQ ID NO: 238 and aFungus comprising a nucleotide sequence at least 97% identical to SEQ IDNO: 326. For example, a complex endophyte may be a combination of aBacterium comprising a nucleotide sequence at least 97% identical to SEQID NO: 239 and a Fungus comprising a nucleotide sequence at least 97%identical to SEQ ID NO: 327. For example, a complex endophyte may be acombination of a Bacterium comprising a nucleotide sequence at least 97%identical to SEQ ID NO: 240 and a Fungus comprising a nucleotidesequence at least 97% identical to SEQ ID NO: 328. For example, acomplex endophyte may be a combination of a Bacterium comprising anucleotide sequence at least 97% identical to SEQ ID NO: 241 and aFungus comprising a nucleotide sequence at least 97% identical to SEQ IDNO: 329. For example, a complex endophyte may be a combination of aBacterium comprising a nucleotide sequence at least 97% identical to SEQID NO: 242 and a Fungus comprising a nucleotide sequence at least 97%identical to SEQ ID NO: 330. For example, a complex endophyte may be acombination of a Bacterium comprising a nucleotide sequence at least 97%identical to SEQ ID NO: 243 and a Fungus comprising a nucleotidesequence at least 97% identical to SEQ ID NO: 331. For example, acomplex endophyte may be a combination of a Bacterium comprising anucleotide sequence at least 97% identical to SEQ ID NO: 244 and aFungus comprising a nucleotide sequence at least 97% identical to SEQ IDNO: 332. For example, a complex endophyte may be a combination of aBacterium comprising a nucleotide sequence at least 97% identical to SEQID NO: 249 and a Fungus comprising a nucleotide sequence at least 97%identical to SEQ ID NO: 333.

In some cases, the complex endophyte, or one or more components thereof,is of monoclonal origin, providing high genetic uniformity of thecomplex endophyte population in an agricultural formulation or within asynthetic seed or plant combination with the endophyte.

In some embodiments, the complex endophyte can be cultured on a culturemedium or can be adapted to culture on a culture medium.

In some embodiments, the compositions provided herein are stable. Theendofungal bacterial endophyte, endofungal fungal endophyte, or complexendophyte may be shelf stable, where at least 10% of the CFUs are viableafter storage in desiccated form (i.e., moisture content of 30% or less)for 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 or greater than 10 weeks at 4° C. orat room temperature. Optionally, a shelf stable formulation is in a dryformulation, a powder formulation, or a lyophilized formulation. In someembodiments, the formulation is formulated to provide stability for thepopulation of endofungal bacterial endophytes, endofungal fungalendophytes, or complex endophytes. In one embodiment, the formulation issubstantially stable at temperatures between about 0° C. and about 50°C. for at least about 1, 2, 3, 4, 5, or 6 days, or 1, 2, 3 or 4 weeks,or 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 months, or one or more years.In another embodiment, the formulation is substantially stable attemperatures between about 4° C. and about 37° C. for at least about 5,10, 15, 20, 25, 30 or greater than 30 days.

Functional Attributes of Complex Endophytes and Endophytic Components

In some cases, the complex endophyte or endophytic component may produceone or more compounds and/or have one or more activities, e.g., one ormore of the following: production of a metabolite, production of aphytohormone such as auxin, production of acetoin, production of anantimicrobial compound, production of a siderophore, production of acellulase, production of a pectinase, production of a chitinase,production of a xylanase, nitrogen fixation, or mineral phosphatesolubilization. For example, a complex endophyte or endophytic componentcan produce a phytohormone selected from the group consisting of anauxin, a cytokinin, a gibberellin, ethylene, a brassinosteroid, andabscisic acid. In one particular embodiment, the complex endophyte orendophytic component produces auxin (e.g., indole-3-acetic acid (IAA)).Production of auxin can be assayed as described herein. Many of themicrobes described herein are capable of producing the plant hormoneauxin indole-3-acetic acid (IAA) when grown in culture. Auxin plays akey role in altering the physiology of the plant, including the extentof root growth. Therefore, in another embodiment, the complex endophyticpopulation is disposed on the surface or within a tissue of the seed orseedling in an amount effective to detectably increase production ofauxin in the agricultural plant when compared with a referenceagricultural plant. In one embodiment, the increased auxin productioncan be detected in a tissue type selected from the group consisting ofthe root, shoot, leaves, and flowers.

In some embodiments, the complex endophyte or endophytic component canproduce a compound with antimicrobial properties. For example, thecompound can have antibacterial properties, as determined by the growthassays provided herein. In one embodiment, the compound withantibacterial properties shows bacteriostatic or bactericidal activityagainst E. coli and/or Bacillus sp. In another embodiment, the complexendophyte or endophytic component produces a compound with antifungalproperties, for example, fungicidal or fungistatic activity against S.cerevisiae and/or Rhizoctonia.

In some embodiments, the complex endophyte or endophytic componentcomprises bacteria capable of nitrogen fixation, and is thus capable ofproducing ammonium from atmospheric nitrogen. The ability of bacteria tofix nitrogen can be confirmed by testing for growth of the bacteria innitrogen-free growth media, for example, LGI media, as described inmethods known in the art.

In some embodiments, the complex endophyte or endophytic component canproduce a compound that increases the solubility of mineral phosphate inthe medium, i.e., mineral phosphate solubilization, for example, usingthe growth assays described herein. In one embodiment, the complexendophyte or endophytic component n produces a compound that allows thebacterium to grow in growth media containing Ca₃HPO₄ as the solephosphate source.

In some embodiments, the complex endophyte or endophytic component canproduce a siderophore. Siderophores are small high-affinity ironchelating agents secreted by microorganisms that increase thebioavailability of iron. Siderophore production by the complex endophyteor endophytic component can be detected using methods known in the art.

In some embodiments, the complex endophyte or endophytic component canproduce a hydrolytic enzyme. For example, in one embodiment, a complexendophyte or endophytic component can produce a hydrolytic enzymeselected from the group consisting of a cellulase, a pectinase, achitinase and a xylanase. Hydrolytic enzymes can be detected usingmethods known in the art.

In some embodiments, the complex endophyte provides an improvedattribute to the component fungus or bacterium. In some cases, thepresence of one organism is beneficial to the other, and can be a resultof any number of mechanisms of either component, or a synergistic effectof the combination of the two organisms. In some embodiments, theimproved attribute is an improved ability of the endophytic bacterium toproduce crystal proteins. In some embodiments, the improved attribute isan improved ability of the host fungus to sporulate.

Combinations of Complex Endophytes and Complex Endophytic Components

Combinations of complex endophytes or endophytic components can beselected by any one or more of several criteria. In one embodiment,compatible complex endophytes or endophytic components are selected. Asused herein, compatibility refers to populations of complex endophytesor endophytic components that do not significantly interfere with thegrowth, propagation, and/or production of beneficial substances of theother. Incompatible populations can arise, for example, where one of thepopulations produces or secrets a compound that is toxic or deleteriousto the growth of the other population(s). Incompatibility arising fromproduction of deleterious compounds/agents can be detected using methodsknown in the art, and as described herein elsewhere. Similarly, thedistinct populations can compete for limited resources in a way thatmakes co-existence difficult.

In another embodiment, combinations are selected on the basis ofcompounds produced by each population of complex endophytes orendophytic components. For example, the first population is capable ofproducing siderophores, and another population is capable of producinganti-fungal compounds. In one embodiment, the first population ofcomplex endophytes or endophytic components is capable of a functionselected from the group consisting of auxin production, nitrogenfixation, production of an antimicrobial compound, siderophoreproduction, mineral phosphate solubilization, cellulase production,chitinase production, xylanase production, and acetoin production. Inanother embodiment, the second population of complex endophytes orendophytic component is capable of a function selected from the groupconsisting of auxin production, nitrogen fixation, production of anantimicrobial compound, siderophore production, mineral phosphatesolubilization, cellulase production, chitinase production, xylanaseproduction, and acetoin production. In still another embodiment, thefirst and second populations are capable of at least one differentfunction.

In still another embodiment, the combinations of complex endophytes orendophytic components are selected for their distinct localization inthe plant after colonization. For example, the first population ofcomplex endophytes or endophytic components can colonize, and in somecases preferentially colonize, the root tissue, while a secondpopulation can be selected on the basis of its preferential colonizationof the aerial parts of the agricultural plant. Therefore, in oneembodiment, the first population is capable of colonizing one or more ofthe tissues selected from the group consisting of a root, shoot, leaf,flower, and seed. In another embodiment, the second population iscapable of colonizing one or more tissues selected from the groupconsisting of root, shoot, leaf, flower, and seed. In still anotherembodiment, the first and second populations are capable of colonizing adifferent tissue within the agricultural plant.

In still another embodiment, combinations of complex endophytes orendophytic components are selected for their ability to confer one ormore distinct fitness traits on the inoculated agricultural plant,either individually or in synergistic association with other endophytes.Alternatively, two or more endophytes induce the colonization of a thirdendophyte. For example, the first population of complex endophytes orendophytic components is selected on the basis that it conferssignificant increase in biomass, while the second population promotesincreased drought tolerance on the inoculated agricultural plant.Therefore, in one embodiment, the first population is capable ofconferring at least one trait selected from the group consisting ofthermal tolerance, herbicide tolerance, drought resistance, insectresistance, fungus resistance, virus resistance, bacteria resistance,male sterility, cold tolerance, salt tolerance, increased yield,enhanced nutrient use efficiency, increased nitrogen use efficiency,increased fermentable carbohydrate content, reduced lignin content,increased antioxidant content, enhanced water use efficiency, increasedvigor, increased germination efficiency, earlier or increased flowering,increased biomass, altered root-to-shoot biomass ratio, enhanced soilwater retention, or a combination thereof. In another embodiment, thesecond population is capable of conferring a trait selected from thegroup consisting of thermal tolerance, herbicide tolerance, droughtresistance, insect resistance, fungus resistance, virus resistance,bacteria resistance, male sterility, cold tolerance, salt tolerance,increased yield, enhanced nutrient use efficiency, increased nitrogenuse efficiency, increased fermentable carbohydrate content, reducedlignin content, increased antioxidant content, enhanced water useefficiency, increased vigor, increased germination efficiency, earlieror increased flowering, increased biomass, altered root-to-shoot biomassratio, and enhanced soil water retention. In still another embodiment,each of the first and second population is capable of conferring adifferent trait selected from the group consisting of thermal tolerance,herbicide tolerance, drought resistance, insect resistance, fungusresistance, virus resistance, bacteria resistance, male sterility, coldtolerance, salt tolerance, increased yield, enhanced nutrient useefficiency, increased nitrogen use efficiency, increased fermentablecarbohydrate content, reduced lignin content, increased antioxidantcontent, enhanced water use efficiency, increased vigor, increasedgermination efficiency, earlier or increased flowering, increasedbiomass, altered root-to-shoot biomass ratio, and enhanced soil waterretention.

The combinations of complex endophytes or endophytic components can alsobe selected based on combinations of the above criteria. For example,the first population of complex endophytes or endophytic components canbe selected on the basis of the compound it produces (e.g., its abilityto fix nitrogen, thus providing a potential nitrogen source to theplant), while the second population can be selected on the basis of itsability to confer increased resistance of the plant to a pathogen (e.g.,a fungal pathogen).

In some aspects of the present invention, it is contemplated thatcombinations of complex endophytes or endophytic components can providean increased benefit to the host plant, as compared to that conferred bya single endophyte, by virtue of additive effects. For example, oneendophyte strain that induces a benefit in the host plant may inducesuch benefit equally well in a plant that is also colonized with adifferent endophyte strain that also induces the same benefit in thehost plant. The host plant thus exhibits the same total benefit from theplurality of different endophyte strains as the additive benefit toindividual plants colonized with each individual endophyte of theplurality. In one example, a plant is colonized with two differentendophyte strains: one provides a 1× increase in seed protein contentwhen associated with the plant, and the other provides a 2× increase inseed protein content when associated with a different plant. When bothendophyte strains are associated with the same plant, that plant wouldexperience a 3× (additive of 1×+2× single effects) increase in seedprotein content. Additive effects are a surprising aspect of the presentinvention, as non-compatibility of endophytes may result in acancelation of the beneficial effects of both endophytes.

In some aspects of the present invention, it is contemplated that acombination of complex endophytes or endophytic components can providean increased benefit to the host plant, as compared to that conferred bya single endophyte, by virtue of synergistic effects. For example, oneendophyte strain that induces a benefit in the host plant may inducesuch benefit beyond additive effects in a plant that is also colonizedwith a different endophyte strain that also induces that benefit in thehost plant. The host plant thus exhibits the greater total benefit fromthe plurality of different endophyte strains than would be expected fromthe additive benefit of individual plants colonized with each individualendophyte of the plurality. In one example, a plant is colonized withtwo different endophyte strains: one provides a 1× increase in seedprotein content when associated with a plant, and the other provides a2× increase in seed protein content when associated with a differentplant. When both endophyte strains are associated with the same plant,that plant would experience a 5× (greater than an additive of 1×+2×single effects) increase in seed protein content. Synergistic effectsare a surprising aspect of the present invention.

Complex Endophytes and Synthetic Combinations with Plants and PlantElements

It is contemplated that the methods and compositions of the presentinvention may be used to improve any characteristic of any agriculturalplant. The methods described herein can also be used with transgenicplants containing one or more exogenous transgenes, for example, toyield additional trait benefits conferred by the newly introducedendophytic microbes. Therefore, in one embodiment, a plant element of atransgenic maize, wheat, rice, cotton, canola, alfalfa, or barley plantis contacted with a complex endophyte or endophytic component(s).

In some embodiments, the present invention contemplates the use ofcomplex endophytes or endophytic components that can confer a beneficialagronomic trait upon the plant element or resulting plant with which itis associated.

In some cases, the complex endophytes or endophytic components describedherein are capable of moving from one tissue type to another. Forexample, the present invention's detection and isolation of complexendophytes or endophytic components within the mature tissues of plantsafter coating on the exterior of a seed demonstrates their ability tomove from seed exterior into the vegetative tissues of a maturing plant.Therefore, in one embodiment, the population of complex endophytes orendophytic components is capable of moving from the seed exterior intothe vegetative tissues of a plant. In one embodiment, the complexendophyte or endophytic component which is coated onto the seed of aplant is capable, upon germination of the seed into a vegetative state,of localizing to a different tissue of the plant. For example, thecomplex endophyte or endophytic component can be capable of localizingto any one of the tissues in the plant, including: the root,adventitious root, seminal root, root hair, shoot, leaf, flower, bud,tassel, meristem, pollen, pistil, ovaries, stamen, fruit, stolon,rhizome, nodule, tuber, trichome, guard cells, hydathode, petal, sepal,glume, rachis, vascular cambium, phloem, and xylem. In one embodiment,the complex endophyte or endophytic component is capable of localizingto the root and/or the root hair of the plant. In another embodiment,the complex endophyte or endophytic component is capable of localizingto the photosynthetic tissues, for example, leaves and shoots of theplant. In other cases, the complex endophyte or endophytic component islocalized to the vascular tissues of the plant, for example, in thexylem and phloem. In still another embodiment, the complex endophyte iscapable of localizing to the reproductive tissues (flower, pollen,pistil, ovaries, stamen, fruit) of the plant. In another embodiment, thecomplex endophyte or endophytic component is capable of localizing tothe root, shoots, leaves and reproductive tissues of the plant. In stillanother embodiment, the complex endophyte or endophytic componentcolonizes a fruit or seed tissue of the plant. In still anotherembodiment, the complex endophyte or endophytic component is able tocolonize the plant such that it is present in the surface of the plant(i.e., its presence is detectably present on the plant exterior, or theepisphere of the plant). In still other embodiments, the complexendophyte or endophytic component is capable of localizing tosubstantially all, or all, tissues of the plant. In certain embodiments,the complex endophyte or endophytic component is not localized to theroot of a plant. In other cases, the complex endophyte or endophyticcomponent is not localized to the photosynthetic tissues of the plant.

In some cases, the complex endophytes or endophytic components arecapable of replicating within the host plant and colonizing the plant.

In some embodiments, the complex endophytes or endophytic componentsdescribed herein are capable of colonizing a host plant. Successfulcolonization can be confirmed by detecting the presence of the fungalpopulation within the plant. For example, after applying the bacteria tothe seeds, high titers of the fungus can be detected in the roots andshoots of the plants that germinate from the seeds. Detecting thepresence of the complex endophyte or endophytic component inside theplant can be accomplished by measuring the viability of the complexendophyte after surface sterilization of the seed or the plant: complexendophytic colonization results in an internal localization of thecomplex endophyte or one of its components, rendering it resistant toconditions of surface sterilization. The presence and quantity of thecomplex endophyte or endophytic component can also be established usingother means known in the art, for example, immunofluorescence microscopyusing microbe-specific antibodies, or fluorescence in situ hybridization(see, for example, Amann et al. (2001) Current Opinion in Biotechnology12:231-236, incorporated herein by reference in its entirety).Alternatively, specific nucleic acid probes recognizing conservedsequences from an endofungal bacterial endophyte can be employed toamplify a region, for example by quantitative PCR, and correlated toCFUs by means of a standard curve.

In some cases, plants are inoculated with complex endophytes orendophytic components that are isolated from the same species of plantas the plant element of the inoculated plant. For example, a complexendophyte or endophytic component that is normally found in one varietyof Zea mays (corn) is associated with a plant element of a plant ofanother variety of Zea mays that in its natural state lacks said complexendophyte or endophytic component. In one embodiment, the complexendophyte or endophytic component is derived from a plant of a relatedspecies of plant as the plant element of the inoculated plant. Forexample, a complex endophyte or endophytic component that is normallyfound in Zea diploperennis Iltis et al., (diploperennial teosinte) isapplied to a Zea mays (corn), or vice versa. In some cases, plants areinoculated with complex endophytes or endophytic components that areheterologous to the plant element of the inoculated plant. In oneembodiment, the complex endophyte or endophytic component is derivedfrom a plant of another species. For example, a complex endophyte thatis normally found in dicots is applied to a monocot plant (e.g.,inoculating corn with a soy bean-derived endophyte), or vice versa. Inother cases, the complex endophyte or endophytic component to beinoculated onto a plant is derived from a related species of the plantthat is being inoculated. In one embodiment, the complex endophyte orendophytic component is derived from a related taxon, for example, froma related species. The plant of another species can be an agriculturalplant.

In another embodiment, the complex endophyte or endophytic component isdisposed, for example, on the surface of a reproductive element of anagricultural plant, in an amount effective to be detecTable In themature agricultural plant. In one embodiment, the endophyte is disposedin an amount effective to be detecTable In an amount of at least about100 CFU between 100 and 200 CFU, at least about 200 CFU, between 200 and300 CFU, at least about 300 CFU, between 300 and 400 CFU, at least about500 CFU, between 500 and 1,000 CFU, at least about 1,000 CFU, between1,000 and 3,000 CFU, at least about 3,000 CFU, between 3,000 and 10,000CFU, at least about 10,000 CFU, between 10,000 and 30,000 CFU, at leastabout 30,000 CFU, between 30,000 and 100,000 CFU, at least about 100,000CFU or more in the mature agricultural plant.

In some cases, the complex endophyte or endophytic component is capableof colonizing particular plant elements or tissue types of the plant. Inone embodiment, the complex endophyte is disposed on the seed orseedling in an amount effective to be detectable within a target tissueof the mature agricultural plant selected from a fruit, a seed, a leaf,or a root, or portion thereof. For example, the complex endophyte orendophytic component can be detected in an amount of at least about 100CFU, between 100 and 200 CFU, at least about 200 CFU, between 200 and300 CFU, at least about 300 CFU, between 300 and 500 CFU, at least about500 CFU, between 500 and 1,000 CFU, at least about 1,000 CFU, between1,000 and 3,000 CFU, at least about 3,000 CFU, between 3,000 and 10,000CFU, at least about 10,000 CFU, between 10,000 CFU and 30,000 CFU, atleast about 30,000 CFU, between about 30,000 and 100,000 CFU, at leastabout 100,000 CFU, or more than 100,000 CFU, in the target tissue of themature agricultural plant.

Endophytes Compatible with Agrichemicals

In certain embodiments, the complex endophyte or endophytic component isselected on the basis of its compatibility with commonly usedagrichemicals. As mentioned earlier, plants, particularly agriculturalplants, can be treated with a vast array of agrichemicals, includingfungicides, biocides (anti-complex agents), herbicides, insecticides,nematicides, rodenticides, fertilizers, and other agents.

In some cases, it can be important for the complex endophyte orendophytic component to be compatible with agrichemicals, particularlythose with fungicidal or anticomplex properties, in order to persist inthe plant although, as mentioned earlier, there are many such fungicidalor anticomplex agents that do not penetrate the plant, at least at aconcentration sufficient to interfere with the complex endophyte.Therefore, where a systemic fungicide or anticomplex agent is used inthe plant, compatibility of the complex endophyte to be inoculated withsuch agents will be an important criterion.

In one embodiment, natural isolates of complex endophytes or endophyticcomponents that are compatible with agrichemicals can be used toinoculate the plants according to the methods described herein. Forexample, complex endophytes or endophytic components that are compatiblewith agriculturally employed fungicides can be isolated by plating aculture of the complex endophytes or endophytic components on a petridish containing an effective concentration of the fungicide, andisolating colonies of the complex endophyte or endophytic component thatare compatible with the fungicide. In another embodiment, a complexendophyte or endophytic component that is compatible with a fungicide isused for the methods described herein.

Fungicide- and bactericide-compatible complex endophytes or endophyticcomponents can also be isolated by selection on liquid medium. Theculture of complex endophytes or endophytic component scan be plated onpetri dishes without any forms of mutagenesis; alternatively, thecomplex endophytes or endophytic components can be mutagenized using anymeans known in the art. For example, complex endophyte or endophyticcomponent cultures can be exposed to UV light, gamma-irradiation, orchemical mutagens such as ethylmethanesulfonate (EMS) prior to selectionon fungicide containing media. Finally, where the mechanism of action ofa particular fungicide or bactericide is known, the target gene can bespecifically mutated (either by gene deletion, gene replacement,site-directed mutagenesis, etc.) to generate a complex endophyte orendophytic component that is resilient against that particular chemical.It is noted that the above-described methods can be used to isolatecomplex endophytes or endophytic components that are compatible withboth fungistatic and fungicidal compounds, as well as bacteriostatic andbactericidal compounds.

It will also be appreciated by one skilled in the art that a plant maybe exposed to multiple types of fungicides or anticomplex compounds,either simultaneously or in succession, for example at different stagesof plant growth. Where the target plant is likely to be exposed tomultiple fungicidal and/or anticomplex agents, a complex endophyte orendophytic component that is compatible with many or all of theseagrichemicals can be used to inoculate the plant. A complex endophyte orendophytic component that is compatible with several fungicidal agentscan be isolated, for example, by serial selection. A complex endophyteor endophytic component that is compatible with the first fungicidalagent can be isolated as described above (with or without priormutagenesis). A culture of the resulting complex endophyte or endophyticcomponent can then be selected for the ability to grow on liquid orsolid media containing the second antifungal compound (again, with orwithout prior mutagenesis). Colonies isolated from the second selectionare then tested to confirm its compatibility to both antifungalcompounds.

Likewise, complex endophytes or endophytic components that arecompatible to biocides (including herbicides such as glyphosate oranticomplex compounds, whether bacteriostatic or bactericidal) that areagriculturally employed can be isolated using methods similar to thosedescribed for isolating fungicide compatible complex endophytes orendophytic components. In one embodiment, mutagenesis of the complexendophyte or endophytic component population can be performed prior toselection with an anticomplex agent. In another embodiment, selection isperformed on the complex endophyte or endophytic component populationwithout prior mutagenesis. In still another embodiment, serial selectionis performed on a complex endophyte or endophytic component: the complexendophyte or endophytic component is first selected for compatibility toa first anticomplex agent. The isolated compatible complex endophyte orendophytic component is then cultured and selected for compatibility tothe second anticomplex agent. Any colony thus isolated is tested forcompatibility to each, or both anticomplex agents to confirmcompatibility with these two agents.

Compatibility with an antimicrobial agent can be determined by a numberof means known in the art, including the comparison of the minimalinhibitory concentration (MIC) of the unmodified and modifiedendophytes. Therefore, in one embodiment, the present inventiondiscloses an isolated complex endophyte or endophytic component, whereinthe endophyte is modified such that it exhibits at least 3 fold greater,for example, at least 5 fold greater, between 5 and 10 fold greater, atleast 10 fold greater, between 10 and 20 fold greater, at least 20 foldgreater, between 20 and 30 fold greater, at least 30 fold greater ormore MIC to an antimicrobial agent when compared with the unmodifiedendophyte.

In a particular embodiment, disclosed herein are complex endophytes andendophytic components with enhanced compatibility to the herbicideglyphosate. In one embodiment, the complex endophyte or endophyticcomponent has a doubling time in growth medium comprising at least 1 mMglyphosate, for example, between 1 mM and 2 mM glyphosate, at least 2 mMglyphosate, between 2 mM and 5 mM glyphosate, at least 5 mM glyphosate,between 5 mM and 10 mM glyphosate, at least 10 mM glyphosate, between 10mM and 15 mM glyphosate, at least 15 mM glyphosate or more, that is nomore than 250%, between 250% and 100%, for example, no more than 200%,between 200% and 175%, no more than 175%, between 175% and 150%, no morethan 150%, between 150% and 125%, or no more than 125%, of the doublingtime of the complex endophyte or endophytic component in the same growthmedium comprising no glyphosate. In one particular embodiment, thecomplex endophyte or endophytic component has a doubling time in growthmedium comprising 5 mM glyphosate that is no more than 150% the doublingtime of the complex endophyte or endophytic component in the same growthmedium comprising no glyphosate.

In another embodiment, the complex endophyte or endophytic component hasa doubling time in a plant tissue comprising at least 10 ppm glyphosate,between 10 and 15 ppm, for example, at least 15 ppm glyphosate, between15 and 10 ppm, at least 20 ppm glyphosate, between 20 and 30 ppm, atleast 30 ppm glyphosate, between 30 and 40 ppm, at least 40 ppmglyphosate or more, that is no more than 250%, between 250% and 200%,for example, no more than 200%, between 200% and 175%, no more than175%, between 175% and 150%, no more than 150%, between 150% and 125%,or no more than 125%, of the doubling time of the endophyte in areference plant tissue comprising no glyphosate. In one particularembodiment, the complex endophyte or endophytic component has a doublingtime in a plant tissue comprising 40 ppm glyphosate that is no more than150% the doubling time of the endophyte in a reference plant tissuecomprising no glyphosate.

The selection process described above can be repeated to identifyisolates of the complex endophyte or endophytic component that arecompatible with a multitude of antifungal or anticomplex agents.

Candidate isolates can be tested to ensure that the selection foragrichemical compatibility did not result in loss of a desiredbioactivity. Isolates of the complex endophyte or endophytic componentthat are compatible with commonly employed fungicides can be selected asdescribed above. The resulting compatible complex endophyte orendophytic component can be compared with the parental complex endophyteon plants in its ability to promote germination.

The agrichemical compatible complex endophytes or endophytic componentsgenerated as described above can be detected in samples. For example,where a transgene was introduced to render the complex endophytecompatible with the agrichemical(s), the transgene can be used as atarget gene for amplification and detection by PCR. In addition, wherepoint mutations or deletions to a portion of a specific gene or a numberof genes results in compatibility with the agrichemical(s), the uniquepoint mutations can likewise be detected by PCR or other means known inthe art. Such methods allow the detection of the complex endophyte evenif it is no longer viable. Thus, commodity plant products produced usingthe agrichemical compatible complex endophytes or endophytic componentsdescribed herein can readily be identified by employing these andrelated methods of nucleic acid detection.

Beneficial Attributes of Synthetic Combinations of Plant Elements andComplex Endophytes or Endophytic Components Improved AttributesConferred by the Complex Endophyte

The present invention contemplates the establishment of a symbiont in aplant element. In one embodiment, the complex endophyte or endophyticcomponent association results in a detectable change to the plantelement, in particular the seed or the whole plant. The detectablechange can be an improvement in a number of agronomic traits (e.g.,improved general health, increased response to biotic or abioticstresses, or enhanced properties of the plant or a plant part, includingfruits and grains). Alternatively, the detectable change can be aphysiological or biological change that can be measured by methods knownin the art. The detectable changes are described in more detail in thesections below. As used herein, a complex endophyte or endophyticcomponent is considered to have conferred an improved agricultural traitwhether or not the improved trait arose from the plant, the complexendophyte, or endophytic component, or the concerted action between anyor all of the preceding. Therefore, for example, whether a beneficialhormone or chemical is produced by the plant or complex endophyte orendophytic component, for purposes of the present invention, the complexendophyte will be considered to have conferred an improved agronomictrait upon the host plant.

In some embodiments, plant-endophyte combinations confer an agronomicbenefit in agricultural plants. In some embodiments, the agronomic traitis selected from the group consisting of altered oil content, alteredprotein content, altered seed carbohydrate composition, altered seed oilcomposition, and altered seed protein composition, chemical tolerance,cold tolerance, delayed senescence, disease resistance, droughttolerance, increased ear weight, growth improvement, health enhancement,heat tolerance, herbicide tolerance, herbivore resistance, improvednitrogen fixation, improved nitrogen utilization, improved nutrient useefficiency, improved root architecture, improved water use efficiency,increased biomass, increased root length, increased seed weight,increased shoot length, increased yield, increased yield underwater-limited conditions, kernel mass, kernel moisture content, metaltolerance, number of ears, number of kernels per ear, number of pods,nutrition enhancement, pathogen resistance, pest resistance,photosynthetic capability improvement, salinity tolerance, stay-green,vigor improvement, increased dry weight of mature seeds, increased freshweight of mature seeds, increased number of mature seeds per plant,increased chlorophyll content, increased seed germination, increasednumber of pods per plant, increased length of pods per plant, reducednumber of wilted leaves per plant, reduced number of severely wiltedleaves per plant, increased number of non-wilted leaves per plant,increased plant height, earlier or increased flowering, increasedprotein content, increased fermentable carbohydrate content, reducedlignin content, male sterility, increased antioxidant content,modulation in the level of a metabolite, a detectable modulation in thelevel of a transcript, and a detectable modulation in the proteomerelative to a reference plant. In other embodiments, at least twoagronomic traits are improved in the agricultural plant.

For example, the endophyte may provide an improved benefit or toleranceto a plant that is of at least 3%, between 3% and 5%, at least 5%,between 5% and 10%, least 10%, between 10% and 15%, for example at least15%, between 15% and 20%, at least 20%, between 20% and 30%, at least30%, between 30% and 40%, at least 40%, between 40% and 50%, at least50%, between 50% and 60%, at least 60%, between 60% and 75%, at least75%, between 75% and 100%, at least 100%, between 100% and 150%, atleast 150%, between 150% and 200%, at least 200%, between 200% and 300%,or at least 300% or more, when compared with uninoculated plants grownunder the same conditions.

In some aspects, provided herein, are methods for producing a seed of aplant with a heritably altered trait. The trait of the plant can bealtered without known genetic modification of the plant genome, andcomprises the following steps. First, a preparation of an isolatedcomplex endophyte or endophytic component that is heterologous to theseed of the plant is provided, and optionally processed to produce acomplex endophyte or endophytic component formulation. The complexendophyte or endophytic component formulation is then contacted with theplant. The plants are then allowed to go to seed, and the seeds arecollected.

Improved General Health

Also described herein are plants, and fields of plants, that areassociated with beneficial complex endophytes or endophytic components,such that the overall fitness, productivity or health of the plant or aportion thereof, is maintained, increased and/or improved over a periodof time. Improvement in overall plant health can be assessed usingnumerous physiological parameters including, but not limited to, height,overall biomass, root and/or shoot biomass, seed germination, seedlingsurvival, photosynthetic efficiency, transpiration rate, seed/fruitnumber or mass, plant grain or fruit yield, leaf chlorophyll content,photosynthetic rate, root length, or any combination thereof. Improvedplant health, or improved field health, can also be demonstrated throughimproved resistance or response to a given stress, either biotic orabiotic stress, or a combination of one or more abiotic stresses, asprovided herein.

Other Abiotic Stresses

Disclosed herein are complex endophyte- or or endophyticcomponent-associated plants with increased resistance to an abioticstress. Exemplary abiotic stresses include, but are not limited to:

Drought and heat tolerance. When soil water is depleted or if water isnot available during periods of drought, crop yields are restricted.Plant water deficit develops if transpiration from leaves exceeds thesupply of water from the roots. The available water supply is related tothe amount of water held in the soil and the ability of the plant toreach that water with its root system. Transpiration of water fromleaves is linked to the fixation of carbon dioxide by photosynthesisthrough the stomata. The two processes are positively correlated so thathigh carbon dioxide influx through photosynthesis is closely linked towater loss by transpiration. As water transpires from the leaf, leafwater potential is reduced and the stomata tend to close in a hydraulicprocess limiting the amount of photosynthesis. Since crop yield isdependent on the fixation of carbon dioxide in photosynthesis, wateruptake and transpiration are contributing factors to crop yield. Plantswhich are able to use less water to fix the same amount of carbondioxide or which are able to function normally at a lower waterpotential have the potential to conduct more photosynthesis and therebyto produce more biomass and economic yield in many agricultural systems.

In some cases, a plant resulting from seeds or other plant componentstreated with the complex endophyte or endophytic component can exhibit aphysiological change, such as a compensation of the stress-inducedreduction in photosynthetic activity (expressed, for example, as ΔFv/Fm)after exposure to heat shock or drought conditions as compared to acorresponding control, genetically identical plant that does not containthe endophytes grown in the same conditions. In some cases, the complexendophyte- or endophytic component-associated plant as disclosed hereincan exhibit an increased change in photosynthetic activity ΔFv(ΔFv/Fm)after heat-shock or drought stress treatment, for example 1, 2, 3, 4, 5,6, 7 days or more after the heat-shock or drought stress treatment, oruntil photosynthesis ceases, as compared with corresponding controlplant of similar developmental stage but not containing the complexendophyte or endophytic component. For example, a plant having a complexendophyte or endophytic component able to confer heat and/ordrought-tolerance can exhibit a ΔFv/Fm of from about 0.1 to about 0.8after exposure to heat-shock or drought stress or a ΔFv/Fm range of fromabout 0.03 to about 0.8 under one day, or 1, 2, 3, 4, 5, 6, 7, or over 7days post heat-shock or drought stress treatment, or untilphotosynthesis ceases. In some embodiments, stress-induced reductions inphotosynthetic activity can be compensated by at least about 0.25% (forexample, at least about 0.5%, between 0.5% and 1%, at least about 1%,between 1% and 2%, at least about 2%, between 2% and 3%, at least about3%, between 3% and 5%, at least about 5%, between 5% and 10%, at leastabout 8%, at least about 10%, between 10% and 15%, at least about 15%,between 15% and 20%, at least about 20%, between 20 and 25%, at leastabout 25%, between 25% and 30%, at least about 30%, between 30% and 40%,at least about 40%, between 40% and 50%, at least about 50%, between 50%and 60%, at least about 60%, between 60% and 75%, at least about 75%,between 75% and 80%, at least about 80%, between 80% and 85%, at leastabout 85%, between 85% and 90%, at least about 90%, between 90% and 95%,at least about 95%, between 95% and 99%, at least about 99%, between 99%and 100%, or at least 100%) as compared to the photosynthetic activitydecrease in a corresponding reference agricultural plant following heatshock conditions. Significance of the difference between complexendophyte- or endophytic component-associated and reference agriculturalplants can be established upon demonstrating statistical significance,for example at p<0.05 with an appropriate parametric or non-parametricstatistic, e.g., Chi-square test, Student's t-test, Mann-Whitney test,or F-test based on the assumption or known facts that theendophyte-associated plant and reference agricultural plant haveidentical or near identical genomes (isoline comparison).

In selecting traits for improving crops, a decrease in water use,without a change in growth would have particular merit in an irrigatedagricultural system where the water input costs were high. An increasein growth without a corresponding jump in water use would haveapplicability to all agricultural systems. In many agricultural systemswhere water supply is not limiting, an increase in growth, even if itcame at the expense of an increase in water use also increases yield.Water use efficiency (WUE) is a parameter often correlated with droughttolerance, and is the CO2 assimilation rate per water transpired by theplant. An increased water use efficiency of the plant relates in somecases to an increased fruit/kernel size or number. Therefore, in someembodiments, the plants described herein exhibit an increased water useefficiency when compared with a reference agricultural plant grown underthe same conditions. For example, the plants grown from the plantelements comprising the complex endophytes or endophytic components canhave at least 3%, between 3% and 5%, at least 5%, between 5% and 10%, atleast 10%, between 10% and 15%, for example at least 15%, between 15%and 20%, at least 20%, between 20% and 30%, at least 30%, between 30%and 40%, at least 40%, between 40% and 50%, at least 50%, between 50%and 60%, at least 60%, between 60% and 75%, at least 75%, between 75%and 100%, or at least 100% higher WUE than a reference agriculturalplant grown under the same conditions. Such an increase in WUE can occurunder conditions without water deficit, or under conditions of waterdeficit, for example, when the soil water content is less than or equalto 60% of water saturated soil, for example, less than or equal to 50%,less than or equal to 40%, less than or equal to 30%, less than or equalto 20%, less than or equal to 10% of water saturated soil on a weightbasis. In a related embodiment, the plant comprising the complexendophytes or endophytic component can have at least 10% higher relativewater content (RWC), for example, at least 3%, between 3% and 5%, atleast 5%, between 5% and 10%, at least 10%, between 10% and 15%, forexample at least 15%, between 15% and 20%, at least 20%, between 20% and30%, at least 30%, between 30% and 40%, at least 40%, between 40% and50%, at least 50%, between 50% and 60%, at least 60%, between 60% and75%, at least 75%, between 75% and 100%, or at least 100% higher RWCthan a reference agricultural plant grown under the same conditions.

In some embodiments, the plants comprise complex endophytes orendophytic components able to increase heat and/or drought-tolerance insufficient quantity, such that increased growth or improved recoveryfrom wilting under conditions of heat or drought stress is observed. Forexample, an endofungal bacterial endophyte population described hereincan be present in sufficient quantity in a plant, resulting in increasedgrowth as compared to a plant that does not contain the endofungalbacterial endophyte, when grown under drought conditions or heat shockconditions, or following such conditions. Increased heat and/or droughttolerance can be assessed with physiological parameters including, butnot limited to, increased height, overall biomass, root and/or shootbiomass, seed germination, seedling survival, photosynthetic efficiency,transpiration rate, seed/fruit number or mass, plant grain or fruityield, leaf chlorophyll content, photosynthetic rate, root length, wiltrecovery, turgor pressure, or any combination thereof, as compared to areference agricultural plant grown under similar conditions. Forexample, the endophyte may provide an improved benefit or tolerance to aplant that is of at least 3%, between 3% and 5%, at least 5%, between 5%and 10%, least 10%, between 10% and 15%, for example at least 15%,between 15% and 20%, at least 20%, between 20% and 30%, at least 30%,between 30% and 40%, at least 40%, between 40% and 50%, at least 50%,between 50% and 60%, at least 60%, between 60% and 75%, at least 75%,between 75% and 100%, at least 100%, between 100% and 150%, at least150%, between 150% and 200%, at least 200%, between 200% and 300%, atleast 300% or more, when compared with uninoculated plants grown underthe same conditions.

Salt Stress. In other embodiments, complex endophytes or endophyticcomponents able to confer increased tolerance to salinity stress can beintroduced into plants. The resulting plants comprising endophytes canexhibit increased resistance to salt stress, whether measured in termsof survival under saline conditions, or overall growth during, orfollowing salt stress. The physiological parameters of plant healthrecited above, including height, overall biomass, root and/or shootbiomass, seed germination, seedling survival, photosynthetic efficiency,transpiration rate, seed/fruit number or mass, plant grain or fruityield, leaf chlorophyll content, photosynthetic rate, root length, orany combination thereof, can be used to measure growth, and comparedwith the growth rate of reference agricultural plants (e.g., isogenicplants without the endophytes) grown under identical conditions. Forexample, the endophyte may provide an improved benefit or tolerance to aplant that is of at least 3%, between 3% and 5%, at least 5%, between 5%and 10%, at least 10%, between 10% and 15%, for example at least 15%,between 15% and 20%, at least 20%, between 20% and 30%, at least 30%,between 30% and 40%, at least 40%, between 40% and 50%, at least 50%,between 50% and 60%, at least 60%, between 60% and 75%, at least 75%,between 75% and 100%, at least 100%, between 100% and 150%, at least150%, between 150% and 200%, at least 200%, between 200% and 300%, atleast 300% or more, when compared with uninoculated plants grown underthe same conditions. In other instances, endophyte-associated plants andreference agricultural plants can be grown in soil or growth mediacomprising different concentration of sodium to establish the inhibitoryconcentration of sodium (expressed, for example, as the concentration inwhich growth of the plant is inhibited by 50% when compared with plantsgrown under no sodium stress). Therefore, in another embodiment, a plantresulting from plant elements comprising a complex endophyte orendophytic component able to confer salt tolerance described hereinexhibits an increase in the inhibitory sodium concentration by at least10 mM, between 10 mM and 15 mM, for example at least 15 mM, between 15mM and 20 mM, at least 20 mM, between 20 mM and 30 mM, at least 30 mM,between 30 mM and 40 mM, at least 40 mM, between 40 mM and 50 mM, atleast 50 mM, between 50 mM and 60 mM, at least 60 mM, between 60 mM and70 mM, at least 70 mM, between 70 mM and 80 mM, at least 80 mM, between80 mM and 90 mM, at least 90 mM, between 90 mM and 100 mM, at least 100mM or more, when compared with the reference agricultural plants.

High Metal Content. Plants are sessile organisms and therefore mustcontend with the environment in which they are placed. Plants haveadapted many mechanisms to deal with chemicals and substances that maybe deleterious to their health. Heavy metals in particular represent aclass of toxins that are highly relevant for plant growth andagriculture, because many of them are associated with fertilizers andsewage sludge used to amend soils and can accumulate to toxic levels inagricultural fields. Therefore, for agricultural purposes, it isimportant to have plants that are able to tolerate soils comprisingelevated levels of toxic heavy metals. Plants cope with toxic levels ofheavy metals (for example, nickel, cadmium, lead, mercury, arsenic, oraluminum) in the soil by excretion and internal sequestration.Endophytes that are able to confer increased heavy metal tolerance maydo so by enhancing sequestration of the metal in certain compartmentsaway from the seed or fruit and/or by supplementing other nutrientsnecessary to remediate the stress. Use of such endophytes in a plantwould allow the development of novel plant-endophyte combinations forpurposes of environmental remediation (also known as phytoremediation).Therefore, in one embodiment, the plant comprising complex endophytes orendophytic components shows increased metal tolerance as compared to areference agricultural plant grown under the same heavy metalconcentration in the soil.

Alternatively, the inhibitory concentration of the heavy metal can bedetermined for a complex endophyte- or endopytic component-associatedplant and compared with a reference agricultural plant under the sameconditions. Therefore, in one embodiment, the plants resulting fromplant elements comprising complex endophytes or endophytic componentsable to confer heavy metal tolerance described herein exhibit anincrease in the inhibitory metal concentration by at least 0.1 mM,between 0.1 mM and 0.3 mM, for example at least 0.3 mM, between 0.3 mMand 0.5 mM, at least 0.5 mM, between 0.5 mM and 1 mM, at least 1 mM,between 1 mM and 2 mM, at least 2 mM, between 2 mM and 5 mM, at least 5mM, between 5 mM and 10 mM, at least 10 mM, between 10 mM and 15 mM, atleast 15 mM, between 15 mM and 20 mM, at least 20 mM, between 20 mM and30 mM, at least 30 mM, between 30 mM and 50 mM, at least 50 mM or more,when compared with the reference agricultural plants.

Finally, plants inoculated with complex endophytes or endophyticcomponents that are able to confer increased metal tolerance exhibit anincrease in overall metal excretion by at least 3%, between 3% and 5%,at least 5%, between 5% and 10%, at least 10%, between 10% and 15%, forexample at least 15%, between 15% and 20%, at least 20%, between 20% and30%, at least 30%, between 30% and 40%, at least 40%, between 40% and50%, at least 50%, between 50% and 60%, at least 60%, between 60% and75%, at least 75%, between 75% and 100%, at least 100%, between 100% and150%, at least 150%, between 150% and 200%, at least 200%, between 200%and 300%, at least 300% or more, when compared with uninoculated plantsgrown under the same conditions.

Low Nutrient Stress. Complex endophytes or endophytic componentsdescribed herein may also confer to the plant an increased ability togrow in nutrient limiting conditions, for example by solubilizing orotherwise making available to the plants macronutrients ormicronutrients that are complexed, insoluble, or otherwise in anunavailable form. In one embodiment, a plant is inoculated with anendophyte that confers increased ability to liberate and/or otherwiseprovide to the plant with nutrients selected from the group consistingof phosphate, nitrogen, potassium, iron, manganese, calcium, molybdenum,vitamins, or other micronutrients. Such a plant can exhibit increasedgrowth in soil comprising limiting amounts of such nutrients whencompared with reference agricultural plant. Differences between theendophyte-associated plant and reference agricultural plant can bemeasured by comparing the biomass of the two plant types grown underlimiting conditions, or by measuring the physical parameters describedabove. Therefore, in one embodiment, the plant comprising endophyteshows increased tolerance to nutrient limiting conditions as compared toa reference agricultural plant grown under the same nutrient limitedconcentration in the soil, as measured for example by increased biomassor seed yield of at least 3%, between 3% and 5%, at least 5%, between 5%and 10%, at least 10%, between 10% and 15%, for example at least 15%,between 15% and 20%, at least 20%, between 20% and 30%, at least 30%,between 30% and 40%, at least 40%, between 40% and 50%, at least 50%,between 50% and 60%, at least 60%, between 60% and 75%, at least 75%,between 75% and 100%, at least 100%, between 100% and 150%, at least150%, between 150% and 200%, at least 200%, between 200% and 300%, atleast 300% or more, when compared with uninoculated plants grown underthe same conditions.

In other embodiments, the plant containing complex endophytes orendophytic components is able to grown under nutrient stress conditionswhile exhibiting no difference in the physiological parameter comparedto a plant that is grown without nutrient stress. In some embodiments,such a plant will exhibit no difference in the physiological parameterwhen grown with 2-5% less nitrogen than average cultivation practices onnormal agricultural land, for example, at least 10%, between 10% and15%, for example at least 15%, between 15% and 20%, at least 20%,between 20% and 30%, at least 30%, between 30% and 40%, at least 40%,between 40% and 50%, at least 50%, between 50% and 60%, at least 60%,between 60% and 75%, at least 75%, or between 75% and 100%, lessnitrogen, when compared with crop plants grown under normal conditionsduring an average growing season. In some embodiments, the microbecapable of providing nitrogen-stress tolerance to a plant isdiazotrophic. In other embodiments, the microbe capable of providingnitrogen-stress tolerance to a plant is non-diazotrophic.

Cold Stress. In some cases, complex endophytes or endophytic componentsdescribed herein can confer to the plant the ability to tolerate coldstress. Many known methods exist for the measurement of a plant'stolerance to cold stress. As used herein, cold stress refers to both thestress induced by chilling (0° C.-15° C.) and freezing (<0° C.). Somecultivars of agricultural plants can be particularly sensitive to coldstress, but cold tolerance traits may be multigenic, making the breedingprocess difficult. Endophytes able to confer cold tolerance can reducethe damage suffered by farmers on an annual basis. Improved response tocold stress can be measured by survival of plants, production ofprotectant substances such as anthocyanin, the amount of necrosis ofparts of the plant, or a change in crop yield loss, as well as thephysiological parameters used in other examples. Therefore, in anembodiment, the plant comprising complex endophytes or endophyticcomponents shows increased cold tolerance exhibits as compared to areference agricultural plant grown under the same conditions of coldstress. For example, the complex endophytes or endophytic components mayprovide an improved benefit or tolerance to a plant that is of at least3%, between 3% and 5%, at least 5%, between 5% and 10%, least 10%,between 10% and 15%, for example at least 15%, between 15% and 20%, atleast 20%, between 20% and 30%, at least 30%, between 30% and 40%, atleast 40%, between 40% and 50%, at least 50%, between 50% and 60%, atleast 60%, between 60% and 75%, at least 75%, between 75% and 100%, atleast 100%, between 100% and 150%, at least 150%, between 150% and 200%,at least 200%, between 200% and 300%, at least 300% or more, whencompared with uninoculated plants grown under the same conditions.

Biotic Stress. In other embodiments, the complex endophyte or endophyticcomponent protects the plant from a biotic stress, for example, insectinfestation, nematode infestation, complex infection, fungal infection,bacterial infection, oomycete infection, protozoal infection, viralinfection, and herbivore grazing, or a combination thereof. For example,the endophyte may provide an improved benefit or tolerance to a plantthat is of at least 3%, between 3% and 5%, at least 5%, between 5% and10%, least 10%, between 10% and 15%, for example at least 15%, between15% and 20%, at least 20%, between 20% and 30%, at least 30%, between30% and 40%, at least 40%, between 40% and 50%, at least 50%, between50% and 60%, at least 60%, between 60% and 75%, at least 75%, between75% and 100%, at least 100%, between 100% and 150%, at least 150%,between 150% and 200%, at least 200%, between 200% and 300%, at least300% or more, when compared with uninoculated plants grown under thesame conditions.

Insect herbivory. There are an abundance of insect pest species that caninfect or infest a wide variety of plants. Pest infestation can lead tosignificant damage. Insect pests that infest plant species areparticularly problematic in agriculture as they can cause serious damageto crops and significantly reduce plant yields. A wide variety ofdifferent types of plant are susceptible to pest infestation includingcommercial crops such as cotton, soybean, wheat, barley, and corn.

In some cases, complex endophytes or endophytic components describedherein may confer upon the host plant the ability to repel insectherbivores. In other cases, endophytes may produce, or induce theproduction in the plant of, compounds which are insecticidal or insectrepellant. The insect may be any one of the common pathogenic insectsaffecting plants, particularly agricultural plants.

The complex endophyte- or endophytic component-associated plant can betested for its ability to resist, or otherwise repel, pathogenic insectsby measuring, for example, insect load, overall plant biomass, biomassof the fruit or grain, percentage of intact leaves, or otherphysiological parameters described herein, and comparing with areference agricultural plant. In an embodiment, the endophyte-associatedplant exhibits increased biomass as compared to a reference agriculturalplant grown under the same conditions (e.g., grown side-by-side, oradjacent to, endophyte-associated plants). In other embodiments, theendophyte-associated plant exhibits increased fruit or grain yield ascompared to a reference agricultural plant grown under the sameconditions (e.g., grown side-by-side, or adjacent to,endophyte-associated plants). In any of the above, the endophyte mayprovide an improved benefit or tolerance to a plant that is of at least3%, between 3% and 5%, at least 5%, between 5% and 10%, least 10%,between 10% and 15%, for example at least 15%, between 15% and 20%, atleast 20%, between 20% and 30%, at least 30%, between 30% and 40%, atleast 40%, between 40% and 50%, at least 50%, between 50% and 60%, atleast 60%, between 60% and 75%, at least 75%, between 75% and 100%, orat least 100%, when compared with uninoculated plants grown under thesame conditions.

Nematodes. Nematodes are microscopic roundworms that feed on the roots,fluids, leaves and stems of more than 2,000 row crops, vegetables,fruits, and ornamental plants, causing an estimated S100 billion croploss worldwide and accounting for 13% of global crop losses due todisease. A variety of parasitic nematode species infect crop plants,including root-knot nematodes (RKN), cyst- and lesion-forming nematodes.Root-knot nematodes, which are characterized by causing root gallformation at feeding sites, have a relatively broad host range and aretherefore parasitic on a large number of crop species. The cyst- andlesion-forming nematode species have a more limited host range, butstill cause considerable losses in susceptible crops.

Signs of nematode damage include stunting and yellowing of leaves, andwilting of the plants during hot periods. Nematode infestation, however,can cause significant yield losses without any obvious above-grounddisease symptoms. The primary causes of yield reduction are due tounderground root damage. Roots infected by SCN are dwarfed or stunted.Nematode infestation also can decrease the number of nitrogen-fixingnodules on the roots, and may make the roots more susceptible to attacksby other soil-borne plant nematodes.

In an embodiment, the complex endophyte- or endophyticcomponent-associated plant has an increased resistance to a nematodewhen compared with a reference agricultural plant. As before with insectherbivores, biomass of the plant or a portion of the plant, or any ofthe other physiological parameters mentioned elsewhere, can be comparedwith the reference agricultural plant grown under the same conditions.Examples of useful measurements include overall plant biomass, biomassand/or size of the fruit or grain, and root biomass. In one embodiment,the endophyte-associated plant exhibits increased biomass as compared toa reference agricultural plant grown under the same conditions (e.g.,grown side-by-side, or adjacent to, the endophyte-associated plants,under conditions of nematode challenge). In another embodiment, theendophyte-associated plant exhibits increased root biomass as comparedto a reference agricultural plant grown under the same conditions (e.g.,grown side-by-side, or adjacent to, the endophyte-associated plants,under conditions of nematode challenge). In still another embodiment,the endophyte-associated plant exhibits increased fruit or grain yieldas compared to a reference agricultural plant grown under the sameconditions (e.g., grown side-by-side, or adjacent to, theendophyte-associated plants, under conditions of nematode challenge). Inany of the above, the endophyte may provide an improved benefit ortolerance to a plant that is of at least 3%, between 3% and 5%, at least5%, between 5% and 10%, least 10%, between 10% and 15%, for example atleast 15%, between 15% and 20%, at least 20%, between 20% and 30%, atleast 30%, between 30% and 40%, at least 40%, between 40% and 50%, atleast 50%, between 50% and 60%, at least 60%, between 60% and 75%, atleast 75%, between 75% and 100%, or at least 100%, when compared withuninoculated plants grown under the same conditions.

Fungal Pathogens. Fungal diseases are responsible for yearly losses ofover S10 Billion on agricultural crops in the US, represent 42% ofglobal crop losses due to disease, and are caused by a large variety ofbiologically diverse pathogens. Different strategies have traditionallybeen used to control them. Resistance traits have been bred intoagriculturally important varieties, thus providing various levels ofresistance against either a narrow range of pathogen isolates or races,or against a broader range. However, this involves the long and laborintensive process of introducing desirable traits into commercial linesby genetic crosses and, due to the risk of pests evolving to overcomenatural plant resistance, a constant effort to breed new resistancetraits into commercial lines is required. Alternatively, fungal diseaseshave been controlled by the application of chemical fungicides. Thisstrategy usually results in efficient control, but is also associatedwith the possible development of resistant pathogens and can beassociated with a negative impact on the environment. Moreover, incertain crops, such as barley and wheat, the control of fungal pathogensby chemical fungicides is difficult or impractical.

The present invention contemplates the use of complex endophytes orendophytic component that are able to confer resistance to fungalpathogens to the host plant. Increased resistance to fungal inoculationcan be measured, for example, using any of the physiological parameterspresented above, by comparing with reference agricultural plants. In anembodiment, the endophyte-associated plant exhibits increased biomassand/or less pronounced disease symptoms as compared to a referenceagricultural plant grown under the same conditions (e.g., grownside-by-side, or adjacent to, the endophyte-associated plants, infectedwith the fungal pathogen). In still another embodiment, theendophyte-associated plant exhibits increased fruit or grain yield ascompared to a reference agricultural plant grown under the sameconditions (e.g., grown side-by-side, or adjacent to, theendophyte-associated plants, infected with the fungal pathogen). Inanother embodiment, the endophyte-associated plant exhibits decreasedhyphal growth as compared to a reference agricultural plant grown underthe same conditions (e.g., grown side-by-side, or adjacent to, theendophyte-associated plants, infected with the fungal pathogen). Forexample, the endophyte may provide an improved benefit to a plant thatis of at least 3%, between 3% and 5%, at least 5%, between 5% and 10%,least 10%, between 10% and 15%, for example at least 15%, between 15%and 20%, at least 20%, between 20% and 30%, at least 30%, between 30%and 40%, at least 40%, between 40% and 50%, at least 50%, between 50%and 60%, at least 60%, between 60% and 75%, at least 75%, between 75%and 100%, at least 100%, between 100% and 150%, at least 150%, between150% and 200%, at least 200%, between 200% and 300%, at least 300% ormore, when compared with uninoculated plants grown under the sameconditions.

Viral Pathogens. Plant viruses are estimated to account for 18% ofglobal crop losses due to disease. There are numerous examples of viralpathogens affecting agricultural productivity. In an embodiment, thecomplex endophyte or endophytic component provides protection againstviral pathogens such that the plant has increased biomass as compared toa reference agricultural plant grown under the same conditions. In stillanother embodiment, the endophyte-associated plant exhibits greaterfruit or grain yield, when challenged with a virus, as compared to areference agricultural plant grown under the same conditions. In yetanother embodiment, the endophyte-associated plant exhibits lower viraltiter, when challenged with a virus, as compared to a referenceagricultural plant grown under the same conditions.

Complex Pathogens. Likewise, bacterial pathogens are a significantproblem negatively affecting agricultural productivity and accountingfor 27% of global crop losses due to plant disease. In an embodiment,the complex endophyte or endophytic component described herein providesprotection against bacterial pathogens such that the plant has greaterbiomass as compared to a reference agricultural plant grown under thesame conditions. In still another embodiment, the endophyte-associatedplant exhibits greater fruit or grain yield, when challenged with acomplex pathogen, as compared to a reference agricultural plant grownunder the same conditions. In yet another embodiment, theendophyte-associated plant exhibits lower complex count, when challengedwith a bacterium, as compared to a reference agricultural plant grownunder the same conditions.

Yield and Biomass improvement. In other embodiments, the improved traitcan be an increase in overall biomass of the plant or a part of theplant, including its fruit or seed. In some embodiments, a complexendophyte or endophytic component is disposed on the surface or within atissue of the plant element in an amount effective to increase thebiomass of the plant, or a part or tissue of the plant grown from theplant element. The increased biomass is useful in the production ofcommodity products derived from the plant. Such commodity productsinclude an animal feed, a fish fodder, a cereal product, a processedhuman-food product, a sugar or an alcohol. Such products may be afermentation product or a fermentable product, one such exemplaryproduct is a biofuel. The increase in biomass can occur in a part of theplant (e.g., the root tissue, shoots, leaves, etc.), or can be anincrease in overall biomass. Increased biomass production, such anincrease meaning at at least 3%, between 3% and 5%, at least 5%, between5% and 10%, least 10%, between 10% and 15%, for example at least 15%,between 15% and 20%, at least 20%, between 20% and 30%, at least 30%,between 30% and 40%, at least 40%, between 40% and 50%, at least 50%,between 50% and 60%, at least 60%, between 60% and 75%, at least 75%,between 75% and 100%, or at least 100%, when compared with uninoculatedplants grown under the same conditions. Such increase in overall biomasscan be under relatively stress-free conditions. In other cases, theincrease in biomass can be in plants grown under any number of abioticor biotic stresses, including drought stress, salt stress, heat stress,cold stress, low nutrient stress, nematode stress, insect herbivorystress, fungal pathogen stress, bacterial pathogen stress, and viralpathogen stress. In some embodiments, a complex endophyte or endophyticcomponent is disposed in an amount effective to increase root biomass byat least 3%, between 3% and 5%, at least 5%, between 5% and 10%, least10%, between 10% and 15%, for example at least 15%, between 15% and 20%,at least 20%, between 20% and 30%, at least 30%, between 30% and 40%, atleast 40%, between 40% and 50%, at least 50%, between 50% and 60%, atleast 60%, between 60% and 75%, at least 75%, between 75% and 100%, orat least 100%, when compared with uninoculated plants grown under thesame conditions, when compared with a reference agricultural plant.

In other cases, a complex endophyte or endophytic component is disposedon the plant element in an amount effective to increase the averagebiomass of the fruit or cob from the resulting plant at least 3%,between 3% and 5%, at least 5%, between 5% and 10%, least 10%, between10% and 15%, for example at least 15%, between 15% and 20%, at least20%, between 20% and 30%, at least 30%, between 30% and 40%, at least40%, between 40% and 50%, at least 50%, between 50% and 60%, at least60%, between 60% and 75%, at least 75%, between 75% and 100%, or atleast 100%, when compared with uninoculated plants grown under the sameconditions.

Increase in plant growth hormones. Many of the microbes described hereinare capable of producing the plant hormone auxin indole-3-acetic acid(IAA) when grown in culture. Auxin may play a key role in altering thephysiology of the plant, including the extent of root growth. Therefore,in other embodiments, a complex endophyte or endophytic component isdisposed on the surface or within a tissue of the plant element in anamount effective to detectably induce production of auxin in theagricultural plant. For example, the increase in auxin production can beat least 2%, at least 3%, at least 4%, at least 5%, at least 6%, atleast 7%, at least 8%, at least 9%, at least 10%, at least 15%, forexample, at least 20%, at least 30%, at least 40%, at least 50%, atleast 60%, at least 75%, at least 100%, or more, when compared with areference agricultural plant. In some embodiments, the increased auxinproduction can be detected in a tissue type selected from the groupconsisting of the root, shoot, leaves, and flowers.

Improvement of Other Traits

In other embodiments, the inoculated complex endophyte or endophyticcomponent can confer other beneficial traits to the plant. Improvedtraits can include an improved nutritional content of the plant or plantpart used for human consumption. In one embodiment, the complexendophyte- or or endophytic component-associated plant is able toproduce a detectable change in the content of at least one nutrient.Examples of such nutrients include amino acid, protein, oil (includingany one of Oleic acid, Linoleic acid, Alpha-linoleic acid, Saturatedfatty acids, Palmitic acid, Stearic acid and Trans fats), carbohydrate(including sugars such as sucrose, glucose and fructose, starch, ordietary fiber), Vitamin A, Thiamine (vit. B1), Riboflavin (vit. B2),Niacin (vit. B3), Pantothenic acid (B5), Vitamin B6, Folate (vit. B9),Choline, Vitamin C, Vitamin E, Vitamin K, Calcium, Iron, Magnesium,Manganese, Phosphorus, Potassium, Sodium, Zinc. In one embodiment, theendophyte-associated plant or part thereof contains at least oneincreased nutrient when compared with reference agricultural plants.

In other cases, the improved trait can include reduced content of aharmful or undesirable substance when compared with referenceagricultural plants. Such compounds include those which are harmful wheningested in large quantities or are bitter tasting (for example, oxalicacid, amygdalin, certain alkaloids such as solanine, caffeine, nicotine,quinine and morphine, tannins, cyanide). As such, in one embodiment, thecomplex endophyte- or endophytic component-associated plant or partthereof contains less of the undesirable substance when compared withreference agricultural plant. In a related embodiment, the improvedtrait can include improved taste of the plant or a part of the plant,including the fruit or seed. In a related embodiment, the improved traitcan include reduction of undesirable compounds produced by otherendophytes in plants, such as degradation of Fusarium-produceddeoxynivalenol (also known as vomitoxin and a virulence factor involvedin Fusarium head blight of maize and wheat) in a part of the plant,including the fruit or seed.

The complex endophyte- or endophytic component-associated plant can alsohave an altered hormone status or altered levels of hormone productionwhen compared with a reference agricultural plant. An alteration inhormonal status may affect many physiological parameters, includingflowering time, water efficiency, apical dominance and/or lateral shootbranching, increase in root hair, and alteration in fruit ripening.

The association between the complex endophyte or endophytic componentand the plant can also be detected using other methods known in the art.For example, the biochemical, metabolomics, proteomic, genomic,epigenomic and/or transcriptomic profiles of complex endophyte- orendophytic component-associated plants can be compared with referenceagricultural plants under the same conditions.

Transcriptome analysis of endophyte-associated and referenceagricultural plants can also be performed to detect changes inexpression of at least one transcript, or a set or network of genes uponendophyte association. Similarly, epigenetic changes can be detectedusing methylated DNA immunoprecipitation followed by high-throughputsequencing.

Metabolomic differences between the plants can be detected using methodsknown in the art. The metabolites, proteins, or other compoundsdescribed herein can be detected using any suitable method including,but not limited to gel electrophoresis, liquid and gas phasechromatography, either alone or coupled to mass spectrometry, NMR,immunoassays (enzyme-linked immunosorbent assays (ELISA)), chemicalassays, spectroscopy, optical imaging techniques (such as magneticresonance spectroscopy (MRS), magnetic resonance imaging (MRI), CATscans, ultra sound, MS-based tissue imaging or X-ray detection methods(e.g., energy dispersive x-ray fluorescence detection)) and the like. Insome embodiments, commercial systems for chromatography and NMR analysisare utilized. Such metabolomic methods can be used to detect differencesin levels in hormone, nutrients, secondary metabolites, root exudates,phloem sap content, xylem sap content, heavy metal content, and thelike. Such methods are also useful for detecting alterations in complexendophyte or endophytic component content and status; for example, thepresence and levels of complex/fungal signaling molecules (e.g.,autoinducers and pheromones), which can indicate the status ofgroup-based behavior of endophytes based on, for example, populationdensity.

In some embodiments, a biological sample (whole tissue, exudate, phloemsap, xylem sap, root exudate, etc.) from endophyte-associated andreference agricultural plants can be analyzed essentially as known inthe art.

In a particular embodiment, the metabolite can serve as a signaling orregulatory molecule. The signaling pathway can be associated with aresponse to a stress, for example, one of the stress conditions selectedfrom the group consisting of drought stress, salt stress, heat stress,cold stress, low nutrient stress, nematode stress, insect herbivorystress, fungal pathogen stress, complex pathogen stress, and viralpathogen stress.

When the inoculated agricultural plant is grown under conditions suchthat the level of one or more metabolites is modulated in the plant,wherein the modulation may indicative of increased resistance to astress selected from the group consisting of drought stress, saltstress, heat stress, cold stress, low nutrient stress, nematode stress,insect herbivory stress, fungal pathogen stress, complex pathogenstress, and viral pathogen stress. The increased resistance can bemeasured at about 10 minutes after applying the stress, between 10minutes and 20 minutes, for example about 20 minutes, between 20 and 30minutes, 30 minutes, between 30 and 45 minutes, about 45 minutes,between 45 minutes and 1 hour, about 1 hour, between 1 and 2 hours,about 2 hours, between 2 and 4 hours, about 4 hours, between 4 and 8hours, about 8 hours, between 8 and 12 hours, about 12 hours, between 12and 16 hours, about 16 hours, between 16 and 20 hours, about 20 hours,between 20 and 24 hours, about 24 hours, between 24 and 36 hours, about36 hours, between 36 and 48 hours, about 48 hours, between 48 and 72hours, about 72 hours, between 72 and 96 hours, about 96 hours, between96 and 120 hours, about 120 hours, between 120 hours and one week, orabout a week after applying the stress.

In some embodiments, metabolites in plants can be modulated by makingsynthetic combinations of plants with complex endophytes or endophyticcomponents. For example, complex endophytes or endophytic components cancause a detectable modulation (e.g., an increase or decrease) in thelevel of various metabolites, e.g., indole-3-carboxylic acid,trans-zeatin, abscisic acid, phaseic acid, indole-3-acetic acid,indole-3-butyric acid, indole-3-acrylic acid, jasmonic acid, jasmonicacid methyl ester, dihydrophaseic acid, gibberellin A3, salicylic acid,upon colonization of a plant.

In some embodiments, complex endophytes or endophytic componentsmodulate the level of the metabolite directly (e.g., the microbesproduces the metabolite, resulting in an overall increase in the levelof the metabolite found in the plant). In other cases, the agriculturalplant, as a result of the association with the complex endophytes orendophytic components, exhibits a modulated level of the metabolite(e.g., the plant reduces the expression of a biosynthetic enzymeresponsible for production of the metabolite as a result of the microbeinoculation). In still other cases, the modulation in the level of themetabolite is a consequence of the activity of both the microbe and theplant (e.g., the plant produces increased amounts of the metabolite whencompared with a reference agricultural plant, and the endophyte alsoproduces the metabolite). Therefore, as used herein, a modulation in thelevel of a metabolite can be an alteration in the metabolite levelthrough the actions of the microbe and/or the inoculated plant.

The levels of a metabolite can be measured in an agricultural plant, andcompared with the levels of the metabolite in a reference agriculturalplant, and grown under the same conditions as the inoculated plant. Theuninoculated plant that is used as a reference agricultural plant is aplant that has not been applied with a formulation with the complexendophytes or endophytic components (e.g., a formulation comprisingcomplex endophytes or endophytic components). The uninoculated plantused as the reference agricultural plant is generally the same speciesand cultivar as, and is isogenic to, the inoculated plant.

The metabolite whose levels are modulated (e.g., increased or decreased)in the endophyte-associated plant may serve as a primary nutrient (i.e.,it provides nutrition for the humans and/or animals who consume theplant, plant tissue, or the commodity plant product derived therefrom,including, but not limited to, a sugar, a starch, a carbohydrate, aprotein, an oil, a fatty acid, or a vitamin) The metabolite can be acompound that is important for plant growth, development or homeostasis(for example, a phytohormone such as an auxin, cytokinin, gibberellin, abrassinosteroid, ethylene, or abscisic acid, a signaling molecule, or anantioxidant). In other embodiments, the metabolite can have otherfunctions. For example, in some embodiments, a metabolite can havebacteriostatic, bactericidal, fungistatic, fungicidal or antiviralproperties. In other embodiments, the metabolite can haveinsect-repelling, insecticidal, nematode-repelling, or nematicidalproperties. In still other embodiments, the metabolite can serve a rolein protecting the plant from stresses, may help improve plant vigor orthe general health of the plant. In yet another embodiment, themetabolite can be a useful compound for industrial production. Forexample, the metabolite may itself be a useful compound that isextracted for industrial use, or serve as an intermediate for thesynthesis of other compounds used in industry. In a particularembodiment, the level of the metabolite is increased within theagricultural plant or a portion thereof such that it is present at aconcentration of at least 0.1 ug/g dry weight, for example, at least 0.3ug/g dry weight, between 0.3 ug/g and 1.0 ug/g dry weight, at least 1.0ug/g dry weight, between 1.0 ug/g and 3.0 ug/g dry weight, at least 3.0ug/g dry weight, between 3.0 ug/g and 10 ug/g dry weight, at least 10ug/g dry weight, between 10 ug/g and 30 ug/g dry weight, at least 30ug/g dry weight, between 30 ug/g and 100 ug/g dry weight, at least 100ug/g dry weight, between 100 ug/g and 300 ug/g dry weight, at least 300ug/g dry weight, between 300 ug/g and 1 mg/g dry weight, or more than 1mg/g dry weight, of the plant or portion thereof.

Likewise, the modulation can be a decrease in the level of a metabolite.The reduction can be in a metabolite affecting the taste of a plant or acommodity plant product derived from a plant (for example, a bittertasting compound), or in a metabolite which makes a plant or theresulting commodity plant product otherwise less valuable (for example,reduction of oxalate content in certain plants, or compounds which aredeleterious to human and/or animal health). The metabolite whose levelis to be reduced can be a compound that affects quality of a commodityplant product (e.g., reduction of lignin levels).

Non-Agricultural Uses of Isolated Complex Endophytes or EndophyticComponents

In one embodiment of the present invention, complex endophytes orendophytic components may be used to improve the efficacy or utility ofapplications in which single microbe types are typically used. Forexample, a process that normally utilizes a particular fungus maybenefit from substitution of a complex endophyte in that process, wherethe complex endophyte comprises that particular fungus as a host thatitself further comprises a component bacterium. In another example, aprocess that normally utilizes a particular bacterium may benefit fromsubstitution of a complex endophyte or endophytic component in thatprocess, which comprises a fungal host that itself further comprisesthat particular bacterium.

It is contemplated that the mechanism of process or applicationimprovement may result from one or more mechanisms, such as but notlimited to: the incorporation of an additional organism (host fungus orcomponent bacterium), a synergy between the two organisms (host fungusand component bacterium), a leveraging of a compound produced by one ofthe organisms that is utilized by the other, an additive effect betweenthe two organisms (host fungus and component bacterium), a protectiveeffect of one organism on the other, the induction, upregulation, ordownregulation of a particular biochemical or metabolic pathway in oneor both organisms, the utilization of a different energy source as aresult of the presence of the other organism, improved survivability ofone or both organisms as a result of their association in ahost:component relationship, or a combination of effects.

In one example, the efficacy or survivability of a Gram-negativebacterium in an application is improved by the substitution of a complexendophyte comprising said gram-negative bacterium. As Gram-negativebacteria cannot make spores and are particularly sensitive todesiccation because of their thinner peptidoglycan layer (the reason whythey do not retain the Gram stain), the potential survivability isdecreased when in a non-endofungal state and improved when inside a hostfungus. Inside the fungus, or inside fungal spores, they have a betterchance of surviving desiccation or other environmental stresses.

In one example, the process of baking bread, brewing beer, or fermentinga fruit or grain for alcohol production, is improved by the substitutionof, or addition of, a complex endophyte or endophytic componentcomprising a component bacterium inside the traditional fungal strain.

In one example, the process pickling or curing foods is improved by thesubstitution of, or addition of, a complex endophyte or endophyticcomponent comprising a host fungus further comprising the traditionalbacterial strain.

In one example, the process of manufacturing or delivering insecticidalbacteria can be improved, by the substitution of, or addition of, acomplex endophyte or endophytic component comprising a host fungusfurther comprising the traditional bacterial strain.

In one example, the process of wastewater treatment can be improved bythe substitution of, or addition of, a complex endophyte or endophyticcomponent comprising a host fungus further comprising the traditionalbacterial strain.

In one example, the process of bioremediation of oils, plastics, orother chemicals can be improved by the substitution of, or addition of,a complex endophyte or endophytic component comprising a host fungusfurther comprising the traditional bacterial strain.

In one example, processes related to water quality improvement can beimproved by the substitution of, or addition of, a complex endophyte orendophytic component comprising a host fungus further comprising thetraditional bacterial strain.

In one example, the process of synthesis of biodegradable plastics canbe improved by the substitution of, or addition of, a complex endophyteor endophytic component comprising a host fungus further comprising thetraditional bacterial strain.

In one example, the process of composting biodegradable substances canbe improved by the substitution of, or addition of, a complex endophyteor endophytic component comprising a host fungus further comprising thetraditional bacterial strain.

In one example, the process of manufacturing or deliveringpharmaceutical compounds for human or animal usage can be improved bythe substitution of, or addition of, a complex endophyte or endophyticcomponent comprising a component bacterium inside the traditional fungalstrain.

In one example, the process of manufacturing industrial compounds (suchas, but not limited to: enzymes, lipases, amylases, pectinases, aminoacids, vitamins, antibiotics, acids, lactic acid, glutamic acid, citricacid alcohols, esters, flavoring agents, preservatives, nitrogen,viruses, sugars, biogas, bioplastic) can be improved by the substitutionof, or addition of, a complex endophyte or endophytic componentcomprising a host fungus further comprising a bacterial strain foreither the traditional bacterium or the traditional fungus.

In one example, the process of producing snow or ice can be improved bythe substitution of, or addition of, a complex endophyte or endophyticcomponent comprising a host fungus further comprising the traditionalbacterial strain.

In one example, the process of manufacturing or deliveringpharmaceutical compounds for human or animal usage can be improved bythe substitution of, or addition of, a complex endophyte or endophyticcomponent comprising a component bacterium inside the traditional fungalstrain.

In one example, the process of manufacturing pharmaceutical compounds(such as, but not limited to: enzymes, amino acids, vitamins,antibiotics, hormones, insulin, human growth hormone, vaccines,preservatives, viruses) can be improved by the substitution of, oraddition of, a complex endophyte or endophytic component comprising ahost fungus further comprising a bacterial strain for either thetraditional bacterium or the traditional fungus.

Formulations for Agricultural Use

The purified populations of complex endophytes or endophytic componentsdescribed herein are intended to be useful in the improvement ofagricultural plants, and as such, may be formulated with othercompositions as part of an agriculturally compatible carrier. Thecarrier composition comprising the endophyte populations may be preparedfor agricultural application as a liquid, a solid, or a gas formulation.

In one aspect, the carrier composition is contemplated as a vehicle fora method of association between the agricultural plant element andpurified endophyte population. It is contemplated that such methods ofassociation between the agricultural plant element and purifiedendophyte population can include, but not be limited to: seed treatment,root wash, seedling soak, foliar application, soil inocula, in-furrowapplication, sidedress application, soil pre-treatment, woundinoculation, drip tape irrigation, vector-mediation via a pollinator,injection, osmopriming, hydroponics, aquaponics, aeroponics.

A variety of applications, including but not limited to single carriercompositions, single methods of association, and combinations of carriercompositions and methods of association, are contemplated. In onenon-limiting example, application of the endophyte population to theplant may be achieved, for example, as a powder for surface depositiononto plant leaves, as a spray to the whole plant or selected plantelement, as part of a drip to the soil or the roots, or as a coatingonto the plant element prior to planting. In another non-limitingexample, a plant element may first become associated with a purifiedendophyte population by virtue of seed treatment with a solid (dry)formulation comprising a purified endophyte population, and upongermination and leaf emergence, the plant then be subjected to a foliarspray of a liquid formulation comprising a purified endophytepopulation. In another non-limiting example, a plant may becomeassociated with a purified endophyte population by virtue of inoculationof the growth medium (soil or hydroponic) with a liquid or solidformulation comprising a purified endophyte population, and be subjectedto repeated (two, three, four, or even five subsequent) inoculationswith a liquid or solid formulation comprising a purified endophytepopulation. Any number of single carrier compositions and single methodsof association, as well as combinations of carrier compositions andmethods of association, are intended to be within the scope of thepresent invention, and as such, the examples given are meant to beillustrative and not limiting to the scope of the invention.

The formulation useful for these embodiments generally and typicallyinclude at least one member selected from the group consisting of: abuffer, a tackifier, a microbial stabilizer, a fungicide, an anticomplexagent, an herbicide, a nematicide, an insecticide, a bactericide, avirucide, a plant growth regulator, a rodenticide, a desiccant, and anutrient.

The carrier can be a solid carrier or liquid carrier, and in variousforms including microspheres, powders, emulsions and the like. Thecarrier may be any one or more of a number of carriers that confer avariety of properties, such as increased stability, wettability, ordispersability. Wetting agents such as natural or synthetic surfactants,which can be nonionic or ionic surfactants, or a combination thereof canbe included in a composition of the invention. Water-in-oil emulsionscan also be used to formulate a composition that includes the purifiedpopulation (see, for example, U.S. Pat. No. 7,485,451, which isincorporated herein by reference in its entirety). Suitable formulationsthat may be prepared include wettable powders, granules, gels, agarstrips or pellets, thickeners, biopolymers, and the like,microencapsulated particles, and the like, liquids such as aqueousflowables, aqueous suspensions, water-in-oil emulsions, etc. Theformulation may include grain or legume products, for example, groundgrain or beans, broth or flour derived from grain or beans, starch,sugar, or oil.

In some embodiments, the agricultural carrier may be soil or a plantgrowth medium. Other agricultural carriers that may be used includewater, fertilizers, plant-based oils, humectants, or combinationsthereof. Alternatively, the agricultural carrier may be a solid, such asdiatomaceous earth, loam, silica, alginate, clay, bentonite,vermiculite, seed cases, other plant and animal products, orcombinations, including granules, pellets, or suspensions. Mixtures ofany of the aforementioned ingredients are also contemplated as carriers,such as but not limited to, pesta (flour and kaolin clay), agar orflour-based pellets in loam, sand, or clay, etc. Formulations mayinclude food sources for the cultured organisms, such as barley, rice,or other biological materials such as seed, plant elements, sugar canebagasse, hulls or stalks from grain processing, ground plant material orwood from building site refuse, sawdust or small fibers from recyclingof paper, fabric, or wood. Other suitable formulations will be known tothose skilled in the art.

In an embodiment, the formulation can include a tackifier, sticker, oradherent. Such agents are useful for combining the complex population ofthe invention with carriers that can contain other compounds (e.g.,control agents that are not biologic), to yield a coating composition.Such compositions help create coatings around the plant or plant elementto maintain contact between the endophyte and other agents with theplant or plant element. In one embodiment, adherents (stickers, ortackifiers) are selected from the group consisting of: alginate, gums,starches, lecithins, formononetin, polyvinyl alcohol, alkaliformononetinate, hesperetin, polyvinyl acetate, cephalins, Gum Arabic,Xanthan Gum, carragennan, PGA, other biopolymers, Mineral Oil,Polyethylene Glycol (PEG), Polyvinyl pyrrolidone (PVP),Arabino-galactan, Methyl Cellulose, PEG 400, Chitosan, Polyacrylamide,Polyacrylate, Polyacrylonitrile, Glycerol, Triethylene glycol, VinylAcetate, Gellan Gum, Polystyrene, Polyvinyl, Carboxymethyl cellulose,Gum Ghatti, and polyoxyethylene-polyoxybutylene block copolymers. Otherexamples of adherent compositions that can be used in the syntheticpreparation include those described in EP 0818135, CA 1229497, WO2013090628, EP 0192342, WO 2008103422 and CA 1041788, each of which isincorporated herein by reference in its entirety.

It is also contemplated that the formulation may further comprise ananti-caking agent.

The formulation can also contain a surfactant, wetting agent,emulsifier, stabilizer, or anti-foaming agent. Non-limiting examples ofsurfactants include nitrogen-surfactant blends such as Prefer 28(Cenex), Surf-N(US), Inhance (Brandt), P-28 (Wilfarm) and Patrol(Helena); esterified seed oils include Sun-It II (AmCy), MSO (UAP),Scoil (Agsco), Hasten (Wilfarm) and Mes-100 (Drexel); andorgano-silicone surfactants include Silwet L77 (UAP), Silikin (Terra),Dyne-Amic (Helena), Kinetic (Helena), Sylgard 309 (Wilbur-Ellis) andCentury (Precision), polysorbate 20, polysorbate 80, Tween 20, Tween 80,Scattics, Alktest TW20, Canarcel, Peogabsorb 80, Triton X-100, Conco NI,Dowfax 9N, Igebapl CO, Makon, Neutronyx 600, Nonipol NO, Plytergent B,Renex 600, Solar NO, Sterox, Serfonic N, T-DET-N, Tergitol NP, Triton N,IGEPAL CA-630, Nonident P-40, Pluronic. In one embodiment, thesurfactant is present at a concentration of between 0.01% v/v to 10%v/v. In another embodiment, the surfactant is present at a concentrationof between 0.1% v/v to 1% v/v. An example of an anti-foaming agent wouldbe Antifoam-C.

In certain cases, the formulation includes a microbial stabilizer. Suchan agent can include a desiccant. As used herein, a “desiccant” caninclude any compound or mixture of compounds that can be classified as adesiccant regardless of whether the compound or compounds are used insuch concentrations that they in fact have a desiccating effect on theliquid inoculant. Such desiccants are ideally compatible with thepopulation used, and should promote the ability of the endophytepopulation to survive application on the seeds and to survivedesiccation. Examples of suitable desiccants include one or more oftrehalose, sucrose, glycerol, and methylene glycol. Other suitabledesiccants include, but are not limited to, non-reducing sugars andsugar alcohols (e.g., mannitol or sorbitol). The amount of desiccantintroduced into the formulation can range from about 5% to about 50% byweight/volume, for example, between about 10% to about 40%, betweenabout 15% and about 35%, or between about 20% and about 30%.

In some cases, it is advantageous for the formulation to contain agentssuch as a fungicide, an anticomplex agent, an herbicide, a nematicide,an insecticide, a plant growth regulator, a rodenticide, a bactericide,a virucide, or a nutrient. Such agents are ideally compatible with theagricultural plant element or seedling onto which the formulation isapplied (e.g., it should not be deleterious to the growth or health ofthe plant). Furthermore, the agent is ideally one which does not causesafety concerns for human, animal or industrial use (e.g., no safetyissues, or the compound is sufficiently labile that the commodity plantproduct derived from the plant contains negligible amounts of thecompound).

Nutrient additives to the formulation may include fertilizercompositions such as, but not limited to, nitrogen, phosphorous, orpotassium.

In the liquid form, for example, solutions or suspensions, endophytepopulations of the present invention can be mixed or suspended in wateror in aqueous solutions. Suitable liquid diluents or carriers includewater, aqueous solutions, petroleum distillates, or other liquidcarriers.

Solid compositions can be prepared by dispersing the endophytepopulations of the invention in and on an appropriately divided solidcarrier, such as peat, wheat, bran, vermiculite, clay, talc, bentonite,diatomaceous earth, fuller's earth, pasteurized soil, and the like. Whensuch formulations are used as wettable powders, biologically compatibledispersing agents such as non-ionic, anionic, amphoteric, or cationicdispersing and emulsifying agents can be used.

The solid carriers used upon formulation include, for example, mineralcarriers such as kaolin clay, pyrophyllite, bentonite, montmorillonite,diatomaceous earth, acid white soil, vermiculite, and pearlite, andinorganic salts such as ammonium sulfate, ammonium phosphate, ammoniumnitrate, urea, ammonium chloride, and calcium carbonate. Also, organicfine powders such as wheat flour, wheat bran, and rice bran may be used.The liquid carriers include vegetable oils such as soybean oil andcottonseed oil, glycerol, ethylene glycol, polyethylene glycol,propylene glycol, polypropylene glycol, etc.

In an embodiment, the formulation is ideally suited for coating of apopulation of endophytes onto plant elements. The endophytes populationsdescribed in the present invention are capable of conferring manyfitness benefits to the host plants. The ability to confer such benefitsby coating the populations on the surface of plant elements has manypotential advantages, particularly when used in a commercial(agricultural) scale.

The endophyte populations herein can be combined with one or more of theagents described above to yield a formulation suitable for combiningwith an agricultural plant element, seedling, or other plant element.Endophyte populations can be obtained from growth in culture, forexample, using a synthetic growth medium. In addition, endophytes can becultured on solid media, for example on petri dishes, scraped off andsuspended into the preparation. Endophytes at different growth phasescan be used. For example, endophytes at lag phase, early-log phase,mid-log phase, late-log phase, stationary phase, early death phase, ordeath phase can be used. Endophytic spores may be used for the presentinvention, for example but not limited to: arthospores, sporangispores,conidia, chlamadospores, pycnidiospores, endospores, zoospores.

The formulations comprising endophyte populations of the presentinvention typically contains between about 0.1 to 95% by weight, forexample, between about 1% and 90%, between about 3% and 75%, betweenabout 5% and 60%, between about 10% and 50% in wet weight of theendophyte population of the present invention.

In one embodiment, it is contemplated that the formulation comprises atleast about 10{circumflex over ( )}2 CFU or spores endophyte populationper mL of liquid formulation, between 10{circumflex over ( )}2 and10{circumflex over ( )}9 CFU or spores per mL, about 10{circumflex over( )}9 CFU or spores per mL, between 10{circumflex over ( )}9 and10{circumflex over ( )}4 CFU or spores per mL, about 10{circumflex over( )}4 CFU or spores per mL, between 10{circumflex over ( )}4 and10{circumflex over ( )}5 CFU or spores per mL, about 10{circumflex over( )}5 CFU or spores per mL, between 10{circumflex over ( )}5 and10{circumflex over ( )}6 and 10{circumflex over ( )}7 CFU or spores permL, about 10{circumflex over ( )}7 CFU or spores per mL, between10{circumflex over ( )}7 and 10{circumflex over ( )}8 CFU or spores permL, about 10{circumflex over ( )}8 CFU or spores per mL, between10{circumflex over ( )}8 and 10{circumflex over ( )}9 CFU or spores permL, or even greater than 10{circumflex over ( )}9 CFU or sporesendophyte population per mL of liquid formulation.

In one embodiment, it is contemplated that the formulation comprises atleast about 10{circumflex over ( )}2 CFU or spores endophyte populationper gram of non-liquid formulation, between 10{circumflex over ( )}2 and10{circumflex over ( )}9 CFU or spores per gram, about 10{circumflexover ( )}9 CFU or spores per gram, between 10{circumflex over ( )}9 and10{circumflex over ( )}4 CFU or spores per gram, about 10{circumflexover ( )}4 CFU or spores per gram, between 10{circumflex over ( )}4 and10{circumflex over ( )}5 CFU or spores per gram, about 10{circumflexover ( )}5 CFU or spores per gram, between 10{circumflex over ( )}5 and10{circumflex over ( )}6 CFU or spores per gram, about 10{circumflexover ( )}6 CFU or spores per gram, between 10{circumflex over ( )}6 and10{circumflex over ( )}7 CFU or spores per gram, 10{circumflex over( )}7 CFU or spores per gram, about 10{circumflex over ( )}7 CFU orspores per gram, between 10{circumflex over ( )}7 and 10{circumflex over( )}8 CFU or spores per gram, about 10{circumflex over ( )}8 CFU orspores per gram, between 10{circumflex over ( )}8 and 10{circumflex over( )}9 CFU or spores per gram, or even greater than 10{circumflex over( )}9 CFU or spores endophyte population per gram of non-liquidformulation.

In one embodiment, it is contemplated that the formulation be applied tothe plant element at about 10{circumflex over ( )}2 CFU or spores/seed,between 10{circumflex over ( )}2 and 10{circumflex over ( )}9 CFU orspores, at least about 10{circumflex over ( )}9 CFU or spores, between10{circumflex over ( )}9 and 10{circumflex over ( )}4 CFU or spores, atleast about 10{circumflex over ( )}4 CFU or spores, between10{circumflex over ( )}4 and 10{circumflex over ( )}5 CFU or spores, atleast about 10{circumflex over ( )}5 CFU or spores, between10{circumflex over ( )}5 and 10{circumflex over ( )}6 CFU or spores, atleast about 10{circumflex over ( )}6 CFU or spores, between10{circumflex over ( )}6 and 10{circumflex over ( )}7 CFU or spores, atleast about 10{circumflex over ( )}7 CFU or spores, between10{circumflex over ( )}7 and 10{circumflex over ( )}8 CFU or spores, oreven greater than 10{circumflex over ( )}8 CFU or spores per seed.

Populations of Plant Elements

In another embodiment, the invention provides for a substantiallyuniform population of plant elements (PEs) comprising two or more PEscomprising the endophytic population, as described herein above.Substantial uniformity can be determined in many ways. In some cases, atleast 10%, between 10% and 20%, for example, at least 20%, between 20%and 30%, at least 30%, between 30% and 40%, at least 40%, between 40%and 50%, at least 50%, between 50% and 60%, at least 60%, between 60%and 70%, at least 70%, between 70% and 75%, at least 75%, between 75%and 80%, at least 80%, between 80% and 90%, at least 90%, between 90%and 95%, at least 95% or more of the PEs in the population, contains theendophytic population in an amount effective to colonize the plantdisposed on the surface of the PEs. In other cases, at least 10%,between 10% and 20%, for example, at least 20%, between 20% and 30%, atleast 30%, between 30% and 40%, at least 40%, between 40% and 50%, atleast 50%, between 50% and 60%, at least 60%, between 60% and 70%, atleast 70%, between 70% and 75%, at least 75%, between 75% and 80%, atleast 80%, between 80% and 90%, at least 90%, between 90% and 95%, atleast 95% or more of the plant element s in the population, contains atleast 1, between 1 and 10, 10, between 10 and 100, or 100 CFU on theplant element surface or per gram of plant element, for example, between100 and 200 CFU, at least 200 CFU, between 200 and 300 CFU, at least 300CFU, between 300 and 1,000 CFU, at least 1,000 CFU, between 1,000 and3,000 CFU, at least 3,000 CFU, between 3,000 and 10,000 CFU, at least10,000 CFU, between 10,000 and 30,000 CFU, at least 30,000 CFU, between30,000 and 100,000 CFU, at least 100,000 CFU, between 100,000 and300,000 CFU, at least 300,000 CFU, between 300,000 and 1,000,000 CFU, orat least 1,000,000 CFU per plant element or more.

In a particular embodiment, the population of plant elements is packagedin a bag or container suitable for commercial sale. Such a bag containsa unit weight or count of the plant elements comprising the endophyticpopulation as described herein, and further comprises a label. In anembodiment, the bag or container contains at least 100 plant elements,between 100 and 1,000 plant elements, 1,000 plant elements, between1,000 and 5,000 plant elements, for example, at least 5,000 plantelements, between 5,000 and 10,000 plant elements, at least 10,000 plantelements, between 10,000 and 20,000 plant elements, at least 20,000plant elements, between 20,000 and 30,000 plant elements, at least30,000 plant elements, between 30,000 and 50,000 plant elements, atleast 50,000 plant elements, between 50,000 and 70,000 plant elements,at least 70,000 plant elements, between 70,000 and 80,000 plantelements, at least 80,000 plant elements, between 80,000 and 90,000, atleast 90,000 plant elements or more. In another embodiment, the bag orcontainer can comprise a discrete weight of plant elements, for example,at least 1 lb, between 1 and 2 lbs, at least 2 lbs, between 2 and 5 lbs,at least 5 lbs, between 5 and 10 lbs, at least 10 lbs, between 10 and 30lbs, at least 30 lbs, between 30 and 50 lbs, at least 50 lbs, between 50and 70 lbs, at least 70 lbs or more. The bag or container comprises alabel describing the plant elements and/or said endophytic population.The label can contain additional information, for example, theinformation selected from the group consisting of: net weight, lotnumber, geographic origin of the plant elements, test date, germinationrate, inert matter content, and the amount of noxious weeds, if any.Suitable containers or packages include those traditionally used inplant seed commercialization. The invention also contemplates othercontainers with more sophisticated storage capabilities (e.g., withmicrobiologically tight wrappings or with gas- or water-proofcontainments).

In some cases, a sub-population of plant elements comprising the complexendophytic population is further selected on the basis of increaseduniformity, for example, on the basis of uniformity of microbialpopulation. For example, individual plant elements of pools collectedfrom individual cobs, individual plants, individual plots (representingplants inoculated on the same day) or individual fields can be testedfor uniformity of microbial density, and only those pools meetingspecifications (e.g., at least 80% of tested plant elements have minimumdensity, as determined by quantitative methods described elsewhere) arecombined to provide the agricultural plant elements sub-population.

The methods described herein can also comprise a validating step. Thevalidating step can entail, for example, growing some plant elementscollected from the inoculated plants into mature agricultural plants,and testing those individual plants for uniformity. Such validating stepcan be performed on individual s plant elements eeds collected fromcobs, individual plants, individual plots (representing plantsinoculated on the same day) or individual fields, and tested asdescribed above to identify pools meeting the required specifications.

In some embodiments, methods described herein include planting asynthetic combination described herein. Suitable planters include an airseeder and/or fertilizer apparatus used in agricultural operations toapply particulate materials including one or more of the following,seed, fertilizer and/or inoculants, into soil during the plantingoperation. Seeder/fertilizer devices can include a tool bar havingground-engaging openers thereon, behind which is towed a wheeled cartthat includes one or more containment tanks or bins and associatedmetering means to respectively contain and meter therefrom particulatematerials. See, e.g., U.S. Pat. No. 7,555,990.

In certain embodiments, a composition described herein may be in theform of a liquid, a slurry, a solid, or a powder (wettable powder or drypowder). In another embodiment, a composition may be in the form of aseed coating. Compositions in liquid, slurry, or powder (e.g., wettablepowder) form may be suitable for coating seeds. When used to coat seeds,the composition may be applied to the seeds and allowed to dry. Inembodiments wherein the composition is a powder (e.g., a wettablepowder), a liquid, such as water, may need to be added to the powderbefore application to a seed.

In still another embodiment, the methods can include introducing intothe soil an inoculum of one or more of the endophyte populationsdescribed herein. Such methods can include introducing into the soil oneor more of the compositions described herein. The inoculum(s) orcompositions may be introduced into the soil according to methods knownto those skilled in the art. Non-limiting examples include in-furrowintroduction, spraying, coating seeds, foliar introduction, etc. In aparticular embodiment, the introducing step comprises in-furrowintroduction of the inoculum or compositions described herein.

In an embodiment, plant elements may be treated with composition(s)described herein in several ways, for example via spraying or dripping.Spray and drip treatment may be conducted by formulating compositionsdescribed herein and spraying or dripping the composition(s) onto aseed(s) via a continuous treating system (which is calibrated to applytreatment at a predefined rate in proportion to the continuous flow ofseed), such as a drum-type of treater. Batch systems, in which apredetermined batch size of seed and composition(s) as described hereinare delivered into a mixer, may also be employed.

In another embodiment, the treatment entails coating plant elements. Onesuch process involves coating the inside wall of a round container withthe composition(s) described herein, adding plant elements, thenrotating the container to cause the plant elements to contact the walland the composition(s), a process known in the art as “containercoating.” Plant elements can be coated by combinations of coatingmethods. Soaking typically entails using liquid forms of thecompositions described. For example, plant elements can be soaked forabout 1 minute to about 24 hours (e.g., for at least 1 min, between 1and 5 min, 5 min, between 5 and 10 min, 10 min, between 10 and 20 min,20 min, between 20 and 40 min, 40 min, between 40 and 80 min, 80 min,between 80 min and 3 hrs, 3 hrs, between 3 hrs and 6 hrs, 6 hr, between6 hrs and 12 hrs, 12 hr, between 12 hrs and 24 hrs, 24 hrs).

Population of Plants/Agricultural Fields

A major focus of crop improvement efforts has been to select varietieswith traits that give, in addition to the highest return, the greatesthomogeneity and uniformity. While inbreeding can yield plants withsubstantial genetic identity, heterogeneity with respect to plantheight, flowering time, and time to seed, remain impediments toobtaining a homogeneous field of plants. The inevitable plant-to-plantvariability is caused by a multitude of factors, including unevenenvironmental conditions and management practices. Another possiblesource of variability can, in some cases, be due to the heterogeneity ofthe complex endophyte or endophytic component population inhabiting theplants. By providing complex endophyte populations onto plantreproductive elements, the resulting plants generated by germinating theplant reproductive elements have a more consistent complex endophyte orendophytic component composition, and thus are expected to yield a moreuniform population of plants.

Therefore, in another embodiment, the invention provides a substantiallyuniform population of plants. The population can include at least 10plants, between 10 and 100 plants, for example, at least 100 plants,between 100 and 300 plants, at least 300 plants, between 300 and 1,000plants, at least 1,000 plants, between 1,000 and 3,000 plants, at least3,000 plants, between 3,000 and 10,000 plants, at least 10,000 plants,between 10,000 and 30,000 plants, at least 30,000 plants, between 30,000and 100,000 plants, at least 100,000 plants or more. The plants arederived from plant reproductive elements comprising endophytepopulations as described herein. The plants are cultivated insubstantially uniform groups, for example in rows, groves, blocks,circles, or other planting layout. The plants are grown from plantreproductive elements comprising the complex endophyte or endophyticcomponent population as described herein. The uniformity of the plantscan be measured in a number of different ways.

The uniformity of the plants can be measured in a number of differentways. In one embodiment, there is an increased uniformity with respectto endophytes within the plant population. For example, in oneembodiment, a substantial portion of the population of plants, forexample at least 10%, between 10% and 20%, at least 20%, between 20% and30%, at least 30%, between 30% and 40%, at least 40%, between 40% and50%, at least 50%, between 50% and 60%, at least 60%, between 60% and70%, at least 70%, between 70% and 75%, at least 75%, between 75% and80%, at least 80%, between 80% and 90%, at least 90%, between 90% and95%, at least 95% or more of the plant elements or plants in apopulation, contains a threshold number of an endophyte population. Thethreshold number can be at least 10 CFU, between 10 and 100 CFU, atleast 100 CFU, between 100 and 300 CFU, for example at least 300 CFU,between 300 and 1,000 CFU, at least 1,000 CFU, between 1,000 and 3,000CFU, at least 3,000 CFU, between 3,000 and 10,000 CFU, at least 10,000CFU, between 10,000 and 30,000 CFU, at least 30,000 CFU, between 30,000and 100,000 CFU, at least 100,000 CFU or more, in the plant or a part ofthe plant. Alternatively, in a substantial portion of the population ofplants, for example, in at least 1%, between 1% and 10%, at least 10%,between 10% and 20%, at least 20%, between 20% and 30%, at least 30%,between 30% and 40%, at least 40%, between 40% and 50%, at least 50%,between 50% and 60%, at least 60%, between 60% and 70%, at least 70%,between 70% and 75%, at least 75%, between 75% and 80%, at least 80%,between 80% and 90%, at least 90%, between 90% and 95%, at least 95% ormore of the plants in the population, the endophyte population that isprovided to the seed or seedling represents at least 0.1%, between 0.1%and 1% at least 1%, between 1% and 5%, at least 5%, between 5% and 10%,at least 10%, between 10% and 20%, at least 20%, between 20% and 30%, atleast 30%, between 30% and 40%, at least 40%, between 40% and 50%, atleast 50%, between 50% and 60%, at least 60%, between 60% and 70%, atleast 70%, between 70% and 80%, at least 80%, between 80% and 90%, atleast 90%, between 90% and 95%, at least 95%, between 95% and 99%, atleast 99%, between 99% and 100%, or 100% of the total endophytepopulation in the plant/seed.

In one embodiment, there is increased genetic uniformity of asubstantial proportion or all detectable complex endophytes within thetaxa, genus, or species of the complex endophyte fungus or componentrelative to an uninoculated control. This increased uniformity can be aresult of the complex endophyte or endophytic component being ofmonoclonal origin or otherwise deriving from a population comprising amore uniform genome sequence and plasmid repertoire than would bepresent in the endophyte population a plant that derives its endophytecommunity largely via assimilation of diverse soil symbionts.

In another embodiment, there is an increased uniformity with respect toa physiological parameter of the plants within the population. In somecases, there can be an increased uniformity in the height of the plantswhen compared with a population of reference agricultural plants grownunder the same conditions. For example, there can be a reduction in thestandard deviation in the height of the plants in the population of atleast 5%, between 5% and 10%, for example, at least 10%, between 10% and15%, at least 15%, between 15% and 20%, at least 20%, between 20% and30%, at least 30%, between 30% and 40%, at least 40%, between 40% and50%, at least 50%, between 50% and 60%, at least 60% or more, whencompared with a population of reference agricultural plants grown underthe same conditions. In other cases, there can be a reduction in thestandard deviation in the flowering time of the plants in the populationof at least 5%, between 5% and 10%, for example, at least 10%, between10% and 15%, at least 15%, between 15% and 20%, at least 20%, between20% and 30%, at least 30%, between 30% and 40%, at least 40%, between40% and 50%, at least 50%, between 50% and 60%, at least 60% or more,when compared with a population of reference agricultural plants grownunder the same conditions.

Commodity Plant Products

The present invention provides a commodity plant product, as well asmethods for producing a commodity plant product, that is derived from aplant of the present invention. As used herein, a “commodity plantproduct” refers to any composition or product that is comprised ofmaterial derived from a plant, seed, plant cell, or plant part of thepresent invention. Commodity plant products may be sold to consumers andcan be viable or nonviable. Nonviable commodity products include but arenot limited to nonviable seeds and grains; processed seeds, seed parts,and plant parts; dehydrated plant tissue, frozen plant tissue, andprocessed plant tissue; seeds and plant parts processed for animal feedfor terrestrial and/or aquatic animal consumption, oil, meal, flour,flakes, bran, fiber, paper, tea, coffee, silage, crushed of whole grain,and any other food for human or animal consumption; and biomasses andfuel products; and raw material in industry. Industrial uses of oilsderived from the agricultural plants described herein includeingredients for paints, plastics, fibers, detergents, cosmetics,lubricants, and biodiesel fuel. Soybean oil may be split,inter-esterified, sulfurized, epoxidized, polymerized, ethoxylated, orcleaved. Designing and producing soybean oil derivatives with improvedfunctionality and improved oliochemistry is a rapidly growing field. Thetypical mixture of triglycerides is usually split and separated intopure fatty acids, which are then combined with petroleum-derivedalcohols or acids, nitrogen, sulfonates, chlorine, or with fattyalcohols derived from fats and oils to produce the desired type of oilor fat. Commodity plant products also include industrial compounds, suchas a wide variety of resins used in the formulation of adhesives, films,plastics, paints, coatings and foams.

Although the present invention has been described in detail withreference to examples below, it is understood that various modificationscan be made without departing from the spirit of the invention. Forinstance, while the particular examples below may illustrate the methodsand embodiments described herein using a specific plant, the principlesin these examples may be applied to any agricultural crop. Therefore, itwill be appreciated that the scope of this invention is encompassed bythe embodiments of the inventions recited herein and the specificationrather than the specific examples that are exemplified below. All citedpatents and publications referred to in this application are hereinincorporated by reference in their entirety.

EXAMPLES

Below are examples of specific embodiments for carrying out the presentinvention. The examples are offered for illustrative purposes only, andare not intended to limit the scope of the present invention in any way.Efforts have been made to ensure accuracy with respect to numbers used(e.g., amounts, temperatures, etc.), but some experimental error anddeviation should, of course, be allowed for.

Example 1: Isolation of Plant-Derived Complex Endophytes

Isolation followed the methods described in Hoffman and Arnold (2010,Appl. Environ. Microbiol. 76: 4063-4075). Briefly, fresh, asymptomatictissue was collected from at least three healthy, mature individuals ofeach focal species. Material was transferred to the laboratory forprocessing within 6 to 12 h of collection. Tissue samples were washed inrunning tap water and then cut into 2-mm segments. Segments were surfacesterilized by rinsing in 95% ethanol for 30 s, 10% Clorox (0.6% sodiumhypochlorite) for 2 min, and 70% ethanol for 2 min, allowed to surfacedry under sterile conditions, and plated on 2% malt extract agar (MEA),which encouraged growth by a diversity of endophytes.

Example 2: Identification of Complex Endophyte Host Fungi, EndofungalBacteria, and Endofungal Fungi

Total genomic DNA was extracted from individual fungal isolates obtainedas described above, using the Qiagen DNeasy Plant Mini Kit. PCR was usedto amplify the nuclear ribosomal internal transcribed spacers (ITS) andthe 5.8S gene (ITS ribosomal DNA [rDNA]) and when possible the first 600bp of the large subunit (LSU rDNA) as a single fragment (ca. 1,000 to1,200 bp in length) using the primers ITS1F and ITS4 or LR3. Each 25microliter reaction mixture included 22.5 microliters of InvitrogenPlatinum Taq supermix, 0.5 microliter of each primer (10 uM), and 1.5microliter of DNA template (˜2-4 ng). Cycling reactions were run with MJResearch PTC thermocyclers and consisted of 94° C. for 5 min, 35 cyclesof 94° C. for 30 s, 54° C. for 30 s, and 72° C. for 1 min, and 72° C.for 10 min. Sanger sequencing was performed using an ABI 3730×1 DNAAnalyzers for capillary electrophoresis and fluorescent dye terminatordetection. Sequences were compared with available sequences in GenBankusing BLAST and a 97% similarity with 100% coverage is used as a cutoffthreshold for species assignment.

The presence or absence of bacteria within the surrounding matrix wasdetermined initially using light microscopy. Fungal isolates wereexamined after 1 week of growth in pure culture on 2% MEA using a lightmicroscope with bright-field imaging (400×; numerical aperture[NA]=0.75). Once visual examination ruled out non-endofungal bacteria(i.e., contaminants in the medium or microbes on fungal surfaces), totalgenomic DNA extracted from fresh mycelia was examined using PCR primersspecific to bacterial 16S rRNA genes, 27F and 1429R (1,402 bp). PCRmixes, cycling parameters and sequencing were as described above, exceptthat annealing temperature was 55° C.

Colony PCR was performed on isolates of bacteria from supernatants ofmycelial centrifugation (see above), by gently touching the surface of acolony with a sterile toothpick and using it to stir 2 microliters ofnuclease-free water that then are used as a template for a 25 microliterPCR. The PCR, cycling parameters and sequencing were performed asdescribed above using the 16S bacterial primers. Sequences were comparedwith the ones obtained from fungal total genomic DNA and with thosedeposited in GenBank using BLAST.

Bacterial endophytes of the present invention that are contemplated asbeing capable of functioning as component bacteria in a complexendophyte are described by their characteristic 16S sequences SEQ ID NO:1 to 249 in Table 1.

Fungal endophytes of the present invention that are contemplated asbeing capable of functioning as host fungi in a complex endophyte aredescribed by their characteristic ITS or LSU sequences SEQ ID NO: 250through 333 in Table 2.

Some examples (non-limiting) of complex endophytes of the presentinvention, that comprise a host fungus further comprising a componentbacterium, are described in Table 3.

Specific endophytes that were used as exemplary complex endophytes,along with their corresponding component bacteria, tested by themethodologies in the following examples are listed and described inTable 4.

Example 3: Characterization of Complex Endophytes

Complex endophytes have unique properties or may produce uniquesubstances that may be beneficial to a plant. Even if an endofungalbacterial endophyte has previously been characterized, its introductioninto a host fungus may change its behavior, especially by adding novelfunctions to the symbiotic coupling. The in vitro activities of complexendophytes can be tested using the following colorimetric orgrowth-based assays. Host fungi, endofungal bacterial endophytes, andendofungal fungal endophytes may also be tested using these assays.

Growth on Nitrogen Free LGI Media

All glassware is cleaned with 6M HCl before media preparation. A new 48well plate (600 microliter well volume) is filled with 500microliters/well of sterile LGI agar [per L, 50 g Sucrose, 0.01 gFeCl3-6H2O, 0.02 g CaCl2, 0.8 g K3PO4, 0.2 g CaCl2, 0.2 g MgSO4-7H2O,0.002 g Na2MoO4-2H2O, Agar 15 g, pH 7.5]. Microbes are inoculated intothe 48 wells with a flame-sterilized metal loop. The plate is sealedwith a breathable membrane, incubated at 28° C. for 3 days, and OD600readings taken with a 48 well plate reader.

ACC Deaminase Activity

Microbes are assayed for growth with ACC as their sole source ofnitrogen. Prior to media preparation all glassware is cleaned with 6 MHCl. A 2 M filter sterilized solution of ACC (#1373A, Research Organics,USA) is prepared in water. 2 microliters/mL of this is added toautoclaved LGI agar (see above), and 500 microliter aliquots are placedin a brand new (clean) 48 well plate. The plate is inoculated with aflame sterilized loop, sealed with a breathable membrane, incubated at28° C. for 3 days, and OD600 readings taken. Only wells that weresignificantly more turbid than their corresponding nitrogen free LGIwells are considered to display ACC deaminase activity.

Mineral Phosphate Solubilization

Microbes are plated on tricalcium phosphate media. This is prepared asfollows: 10 g/L glucose, 0.373 g/L NH4NO3, 0.41 g/L MgSO4, 0.295 g/LNaCl, 0.003 FeCl3, 0.7 g/L Ca₃HPO₄, 100 mM Tris and 20 g/L Agar, pH 7,then autoclaved and poured into square Petri plates. After 3 days ofgrowth at 28° C. in darkness, clear halos are measured around coloniesthat are able to solubilize the tricalcium phosphate.

Acetoin and Diacetyl Production

500 ml of autoclaved R2 broth supplemented with 0.5% glucose arealiquoted into a 48 well plate (#07-200-700, Fisher). Microbes areinoculated using a flame-sterilized metal loop, sealed with a breathablemembrane, then incubated for 3 days at 28° C. At day 3, 100microliters/well is added of freshly blended Barritt's Reagents A and B[5 g/L creatine mixed 3:1 (v/v) with freshly prepared ∝-naphthol (75 g/Lin 2.5 M sodium hydroxide)]. After 15 minutes, plates are scored for redor pink colouration relative to a copper coloured negative control(measured as 525 nm absorption on a plate reader).

Auxin Production

500 ml of autoclaved R2 broth supplemented with L-tryptophan to a finalconcentration of 5 mM are autoclaved and poured into a 48 well plate.Using a flame-sterilized loop, all microbes are inoculated into theplate from a fungal stock. The plate is incubated at 28° C. for 3 days,measured for OD525 and OD600 (to asses fungal growth) and finally, 100microliters per well of Salkowski reagent (0.01 M ferric chloride in 35%perchloric acid, #311421, Sigma) is added. After 15 minutes, plates werescored for red or pink coloration relative to a clear-colored negativecontrols (measured as 540 nm absorption on a plate reader).

Siderophore Production

To ensure no contaminating iron is carried over from previousexperiments, all glassware is deferrated with 6 M HCl and water prior tomedia preparation. In this cleaned glassware, R2 broth media, which isiron-limited, is prepared and poured (500 microliters/well) into 48 wellplates and the plate then inoculated with fungi using a flame sterilizedmetal loop. After 3 days of incubation at 28° C., to each well is added200 microliters of O-CAS preparation without gelling agent. Again usingthe cleaned glassware, 1 liter of O-CAS overlay is made by mixing 60.5mg of Chrome azurol S (CAS), 72.9 mg of hexadecyltrimethyl ammoniumbromide (HDTMA), 30.24 g of finely crushedPiperazine-1,4-bis-2-ethanesulfonic acid (PIPES) with 10 ml of 1 mMFeCl3.6H2O in 10 mM HCl solvent. The PIPES has to be finely powdered andmixed gently with stirring (not shaking) to avoid producing bubbles,until a dark blue colour is achieved. 15 minutes after adding thereagent to each well, color change is scored by looking for purple halos(catechol type siderophores) or orange colonies (hydroxamatesiderophores) relative to the deep blue of the 0-Cas.

Antibiosis

Agar plates containing bacteria or yeast in the agar are prepared firstby adding fresh overnight cultures of E. coli DH5a or Saccharomycescerevisiae (yeast) to agar. These are first diluted to OD600=0.2, then 1microliter/mL of this blended into sterile, cool to the touch, but stillliquid R2A agar. These are poured into square Petri dishes, which arethen inoculated when solid by using a flame-sterilized metal loop andgrown for 3 days at 28° C. At this time, plates are scanned andantibiosis is scored by looking for clear halos around fungal colonies.

Phenotype

Colonies of complex endophytes and individual component bacteria wereplated out on agar and grown for 3 days at 28° C. Plates werephotographed and phenotypic characteristics were noted. All results areshown in FIG. 1.

Example 4: Creation of Complex Endophyte and Plant Element Associations

Untreated soy and wheat seeds were surface sterilized using chlorinefumes. Briefly, Erlenmyer flasks containing seeds and a bottle with 100mL of fresh bleach solution were placed in a desiccation jar located ina fume hood Immediately prior to closing the lid of the desiccation jar,3 mL hydrochloric acid was carefully pipetted into the bleach.Sterilization was done for 17 hours for soy and 16 hours for wheat. Uponcompletion the flasks with seeds were removed, sealed in sterile foil,and opened in a sterile biosafety cabinet or laminar flow hood forsubsequent work.

Seeds were coated with endophytes as follows. 2% sodium alginate (SA)was prepared and autoclaved. An Erlenmeyer flask was filled withappropriate amount of deionized water and warmed to about 50 degrees ona heat plate with agitation using stirring bar. SA powder was pouredslowly until it all dissolved. The solution was autoclaved at 121° C.@15 PSI for 30 minutes.

Talcum powder was autoclaved in a dry cycle (121° C. @ 15 PSI for 30minutes) and aliquoted in Ziploc bags or 50 ml falcon tubes.

Endophyte inocula were prepared in the amounts indicated below. Forcontrols, fungal powder was substituted with talc, or liquid fungus withthe liquid medium (Yeast Extract Peptone Broth), respectively.

For fungal powder seed treatment, seeds were placed in a large plasticcontainer. 50 mL of the 2% SA was applied per kilogram of seeds to betreated. The container was covered with a hinged lid and shaken slowlyin orbital motion for about 20 seconds to disperse the SA. 12.5 g offungal powder was premixed with 137.5 g of talcum powder, per kg of seedto be treated. A mixture of the fungal inocula and talc was dispersedevenly on top of the seeds, the container covered, and the seeds shakenslowly in orbital motion for about 20 seconds. Excess powder was sievedoff and the seeds packed in paper bags for storage prior to planting.

For fungal liquid seed treatment, seeds were placed in a large plasticcontainer. 25 ml of 2% SA per kg of seed and the same amount of fungalculture (25 ml per kg of seed) was poured on the seeds. The containerwas covered with a hinged lid and shaken slowly in orbital motion forabout 20 seconds to disperse the SA. 137.5 g of talcum powder per kg ofseed was added and dispersed evenly, the container covered, and theseeds shaken slowly in orbital motion for about 20 seconds. Excessformulation was sieved off and the seeds packed in paper bags forstorage prior to planting.

It is contemplated that the described method may be utilized toassociate a complex endophyte, or its native fungal host endophyte, orits bacterial endophyte component, with any plant element. Includedwithin the scope of this invention as non-limiting examples of such aremethods of associating such endophytes with liquid or powderformulations further comprising a complex endophyte, a bacterialendophyte, or a fungal endophyte, with a seed, a root, a tuber, akeikis, a bud, a stem, a leaf, a flower, a bud, a wound on a plant, astolon, a pistil, a stamen, a root nodule, a shoot, a seedling, a fruit,or a whole plant or portion thereof.

Seed Treatment

A complex, fungal, or bacterial endophyte was inoculated onto seeds as aliquid or powder using a range of formulations including the followingcomponents: sodium alginate and/or methyl cellulose as stickers, talcand flowability polymers. Seeds were air dried after treatment andplanted according to common practice for each crop type.

Osmopriming and Hydropriming

A complex, fungal, or bacterial endophyte is inoculated onto seedsduring the osmopriming (soaking in polyethylene glycol solution tocreate a range of osmotic potentials) and/or hydropriming (soaking inde-chlorinated water) process. Osmoprimed seeds are soaked in apolyethylene glycol solution containing a bacterial and/or fungalendophyte for one to eight days and then air dried for one to two days.Hydroprimed seeds are soaked in water for one to eight days containing abacterial and/or fungal endophyte and maintained under constant aerationto maintain a suitable dissolved oxygen content of the suspension untilremoval and air drying for one to two days. Talc and or flowabilitypolymer are added during the drying process.

Foliar Application

A complex, fungal, or bacterial endophyte is inoculated onto abovegroundplant tissue (leaves and stems) as a liquid suspension in dechlorinatedwater containing adjuvants, sticker-spreaders and UV protectants. Thesuspension is sprayed onto crops with a boom or other appropriatesprayer.

Soil Inoculation

A complex, fungal, or bacterial endophyte is inoculated onto soils inthe form of a liquid suspension either; pre-planting as a soil drench,during planting as an in furrow application, or during crop growth as aside-dress. A fungal or bacterial endophyte is mixed directly into afertigation system via drip tape, center pivot or other appropriateirrigation system.

Hydroponic and Aeroponic Inoculation

A complex, fungal, or bacterial endophyte is inoculated into ahydroponic or aeroponic system either as a powder or liquid suspensionapplied directly to the rockwool substrate, or applied to thecirculating or sprayed nutrient solution.

Vector-Mediated Inoculation

A complex, fungal, or bacterial endophyte is introduced in power form ina mixture containing talc or other bulking agent to the entrance of abeehive (in the case of bee-mediation) or near the nest of anotherpollinator (in the case of other insects or birds. The pollinators pickup the powder when exiting the hive and deposit the inoculum directly tothe crop's flowers during the pollination process.

Root Wash

The method includes contacting the exterior surface of a plant's rootswith a liquid inoculant formulation containing a purified bacterialpopulation, a purified fungal population, a purified complex endophytepopulation, or a mixture of any of the preceding. The plant's roots arebriefly passed through standing liquid microbial formulation or liquidformulation is liberally sprayed over the roots, resulting in bothphysical removal of soil and microbial debris from the plant roots, aswell as inoculation with microbes in the formulation.

Seedling Soak

The method includes contacting the exterior surfaces of a seedling witha liquid inoculant formulation containing a purified bacterialpopulation, a purified fungal population, or a mixture of any of thepreceding. The entire seedling is immersed in standing liquid microbialformulation for at least 30 seconds, resulting in both physical removalof soil and microbial debris from the plant roots, as well asinoculation of all plant surfaces with microbes in the formulation.Alternatively, the seedling can be germinated from seed in ortransplanted into media soaked with the microbe(s) of interest and thenallowed to grow in the media, resulting in soaking of the plantlet inmicrobial formulation for much greater time totaling as much as days orweeks. Endophytic microbes likely need time to colonize and enter theplant, as they explore the plant surface for cracks or wounds to enter,so the longer the soak, the more likely the microbes will successfullybe installed in the plant.

Wound Inoculation

The method includes contacting the wounded surface of a plant with aliquid or solid inoculant formulation containing a purified bacterialpopulation, a purified fungal population, or a mixture of any of thepreceding. Plant surfaces are designed to block entry of microbes intothe endosphere, since pathogens attempting to infect plants in this way.In order to introduce beneficial endophytic microbes to plantendospheres, we need a way to access the interior of the plant which wecan do by opening a passage by wounding. This wound can take a number offorms, including pruned roots, pruned branches, puncture wounds in thestem breaching the bark and cortex, puncture wounds in the tap root,puncture wounds in leaves, and puncture wounds seed allowing entry pastthe seed coat. Wounds can be made using needles, hammer and nails,knives, drills, etc. Into the wound can then be contacted the microbialinoculant as liquid, as powder, inside gelatin capsules, in apressurized capsule injection system, in a pressurized reservoir andtubing injection system, allowing entry and colonization by microbesinto the endosphere. Alternatively, the entire wounded plant can besoaked or washed in the microbial inoculant for at least 30 seconds,giving more microbes a chance to enter the wound, as well as inoculatingother plant surfaces with microbes in the formulation—for examplepruning seedling roots and soaking them in inoculant beforetransplanting is a very effective way to introduce endophytes into theplant.

Injection

The method includes injecting microbes into a plant in order tosuccessfully install them in the endosphere. Plant surfaces are designedto block entry of microbes into the endosphere, since pathogensattempting to infect plants in this way. In order to introducebeneficial endophytic microbes to endospheres, we need a way to accessthe interior of the plant which we can do by puncturing the plantsurface with a need and injecting microbes into the inside of the plant.Different parts of the plant can be inoculated this way including themain stem or trunk, branches, tap roots, seminal roots, buttress roots,and even leaves. The injection can be made with a hypodermic needle, adrilled hole injector, or a specialized injection system, and throughthe puncture wound can then be contacted the microbial inoculant asliquid, as powder, inside gelatin capsules, in a pressurized capsuleinjection system, in a pressurized reservoir and tubing injectionsystem, allowing entry and colonization by microbes into the endosphere.

Example 5: Verification of Complex Endophyte Colonization in PlantElements or Whole Plants

The following methods may be used to verify stable integration of thecomplex endophyte or components with the target plant host or targetplant host plant elements, as well as verification of presence of thecomplex endophyte or components that have been transmitted to progeny ofthe target plant host.

Culturing to Confirm Colonization of Plant by Bacteria

The presence of complex endophytes in whole plants or plant elements,such as seeds, roots, leaves, or other parts, can be detected byisolating microbes from plant or plant element homogenates (optionallysurface-sterilized) on antibiotic-free media and identifying visually bycolony morphotype and molecular methods described herein. Representativecolony morphotypes are also used in colony PCR and sequencing forisolate identification via ribosomal gene sequence analysis as describedherein. These trials are repeated twice per experiment, with 5biological samples per treatment.

Culture-Independent Methods to Confirm Colonization of the Plant orSeeds by Complex Endophytes

One way to detect the presence of complex endophytes on or within plantsor seeds is to use quantitative PCR (qPCR). Internal colonization by thecomplex endophyte can be demonstrated by using surface-sterilized planttissue (including seed) to extract total DNA, and isolate-specificfluorescent MGB probes and amplification primers are used in a qPCRreaction. An increase in the product targeted by the reporter probe ateach PCR cycle therefore causes a proportional increase in fluorescencedue to the breakdown of the probe and release of the reporter.Fluorescence is measured by a quantitative PCR instrument and comparedto a standard curve to estimate the number of fungal or bacterial cellswithin the plant.

The design of both species-specific amplification primers, andisolate-specific fluorescent probes are well known in the art. Planttissues (seeds, stems, leaves, flowers, etc.) are pre-rinsed and surfacesterilized using the methods described herein.

Total DNA is extracted using methods known in the art, for example usingcommercially available Plant-DNA extraction kits, or the followingmethod.

1. Tissue is placed in a cold-resistant container and 10-50 mL of liquidnitrogen is applied. Tissues are then macerated to a powder.

2. Genomic DNA is extracted from each tissue preparation, following achloroform:isoamyl alcohol 24:1 protocol (Sambrook, Joseph, Edward F.Fritsch, and Thomas Maniatis. Molecular cloning. Vol. 2. New York: Coldspring harbor laboratory press, 1989.).

Quantitative PCR is performed essentially as described by Gao, Zhan, etal. Journal of clinical microbiology 48.10 (2010): 3575-3581 withprimers and probe(s) specific to the desired isolate (the host fungus,the endofungal bacterial endophyte, or the endofungal fungal endophyte)using a quantitative PCR instrument, and a standard curve is constructedby using serial dilutions of cloned PCR products corresponding to thespecie-specific PCR amplicon produced by the amplification primers. Dataare analyzed using instructions from the quantitative PCR instrument'smanufacturer software.

As an alternative to qPCR, Terminal Restriction Fragment LengthPolymorphism, (TRFLP) can be performed, essentially as described inJohnston-Monje D, Raizada MN (2011) PLoS ONE 6(6): e20396. Groupspecific, fluorescently labeled primers are used to amplify a subset ofthe microbial population, for example bacteria and fungi. Thisfluorescently labeled PCR product is cut by a restriction enzyme chosenfor heterogeneous distribution in the PCR product population. The enzymecut mixture of fluorescently labeled and unlabeled DNA fragments is thensubmitted for sequence analysis on a Sanger sequence platform such asthe Applied Biosystems 3730 DNA Analyzer.

Immunological Methods to Detect Complex Endophytes in Seeds andVegetative Tissues

A polyclonal antibody is raised against specific the host fungus, theendofungal bacterial endophyte, or the endofungal fungal endophyte viastandard methods. Enzyme-linked immunosorbent assay (ELISA) andimmunogold labeling is also conducted via standard methods, brieflyoutlined below.

Immunofluorescence microscopy procedures involve the use of semi-thinsections of seed or seedling or adult plant tissues transferred to glassobjective slides and incubated with blocking buffer (20 mM Tris(hydroxymethyl)-aminomethane hydrochloride (TBS) plus 2% bovine serumalbumin, pH 7.4) for 30 min at room temperature. Sections are firstcoated for 30 min with a solution of primary antibodies and then with asolution of secondary antibodies (goat anti-rabbit antibodies) coupledwith fluorescein isothiocyanate (FITC) for 30 min at room temperature.Samples are then kept in the dark to eliminate breakdown of thelight-sensitive FITC. After two 5-min washings with sterile potassiumphosphate buffer (PB) (pH 7.0) and one with double-distilled water,sections are sealed with mounting buffer (100 mL 0.1 M sodium phosphatebuffer (pH 7.6) plus 50 mL double-distilled glycerine) and observedunder a light microscope equipped with ultraviolet light and a FITCTexas-red filter.

Ultrathin (50- to 70-nm) sections for TEM microscopy are collected onpioloform-coated nickel grids and are labeled with 15-nm gold-labeledgoat anti-rabbit antibody. After being washed, the slides are incubatedfor 1 h in a 1:50 dilution of 5-nm gold-labeled goat anti-rabbitantibody in IGL buffer. The gold labeling is then visualized for lightmicroscopy using a BioCell silver enhancement kit. Toluidine blue(0.01%) is used to lightly counterstain the gold-labeled sections. Inparallel with the sections used for immunogold silver enhancement,serial sections are collected on uncoated slides and stained with 1%toluidine blue. The sections for light microscopy are viewed under anoptical microscope, and the ultrathin sections are viewed by TEM.

Example 6: Demonstration of Phenotypic Alterations of Host Plants Due toPresence of the Complex Endophyte: Germination Assays Testing forGermination Enhancement in Normal Conditions

Standard germination tests are used to assess the ability of the complexendophyte to enhance the seeds' germination and early growth. Briefly,seeds that have been coated with the complex endophyte or bacterialendophyte component as described elsewhere are placed in between wetbrown paper towels. An equal number of seeds obtained from controlplants that do not contain the endophyte (complex or bacterial) retreated in the same way. The paper towels are placed on top of 1×2 feetplastic trays and maintained in a growth chamber set at 25° C. and 70%humidity for 7 days. The proportion of seeds that germinatedsuccessfully is compared between the complex endophyte-treated seeds andthe non-complex endophyte-treated.

Testing for Germination Enhancement Under Biotic Stress

A modification of the method developed by Hodgson [Am. Potato. J. 38:259-264 (1961)] is used to test germination enhancement in complexendophyte-treated seeds under biotic stress. Biotic stress is understoodas a concentration of inocula in the form of cell (bacteria) or sporesuspensions (fungus) of a known pathogen for a particular crop (e.g.,Pantoea stewartii or Fusarium graminearum for Zea mays L.). Briefly, foreach level of biotic stress, seeds that have been treated with complexendophyte strains, and seed controls (lacking the complex endophytestrains), are placed in between brown paper towels. Each one of thereplicates is placed inside a large petri dish (150 mm in diameter). Thetowels are then soaked with 10 mL of pathogen cell or spore suspensionat a concentration of 10{circumflex over ( )}4 to 10{circumflex over( )}8 cells/spores per mL. Each level corresponds with an order ofmagnitude increment in concentration (thus, 5 levels). The petri dishesare maintained in a growth chamber set at 25° C. and 70% humidity for 7days. The proportion of seeds that germinate successfully is comparedbetween the complex endophyte-treated seeds and the non-complexendophyte-treated for each level of biotic stress.

Testing for Germination Enhancement Under Drought Stress

Polyethylene glycol (PEG) is an inert, water-binding polymer with anon-ionic and virtually impermeable long chain [Couper and Eley, J.Polymer Sci., 3: 345-349 (1984)] that accurately mimics drought stressunder dry-soil conditions. The higher the concentration of PEG, thelower the water potential achieved, thus inducing higher water stress ina watery medium. To determine germination enhancement in seeds treatedwith complex endophytes or bacterial endophyte components, the effect ofosmotic potential on germination was tested at a range of waterpotential representative of drought conditions following Perez-Fernandezet al. [J. Environ. Biol. 27: 669-685 (2006)]. The range of waterpotentials simulated those that are known to cause drought stress in arange of cultivars and wild plants, (−0.05 MPa to −5 MPa) [Crain et al.,Nature Climate Change 3: 63-67 (2013)]. The appropriate concentration ofpolyethylene glycol (6000) required to achieve a particular waterpotential was determined following Michel and Kaufmann (Plant Physiol.,51: 914-916 (1973)) and further modifications by Hardegree and Emmerich(Plant Physiol., 92, 462-466 (1990)). The final equation used todetermine amounts of PEG was: Ψ=0.130 [PEG]2 T-13.7 [PEG] 2; where theosmotic potential (Ψ) is a function of temperature (T).

Testing for Germination Enhancement Under Drought Stress (Soybean)

Germination experiments for soybean under drought stress experimentswere performed using sterile heavy weight germination paper immersedwith 8% PEG 6000 solution (Ψ equal to −0.1 MPa; 10 mL solution/plate) in150 mm Petri plates. Surface sterilized soy seeds were first coated with2% sodium alginate to enable microbial adhesion, and then treated withequal volume of microbial culture in a 50 mL Falcon tube. Seeds weremixed for homogenous coating. Seed treatment calculations were based on0.01 mL each of microbial culture and 2% sodium alginate solution forevery one gram of seed. Treated seeds were coated were placed on the PEG6000 saturated germination paper and incubated in the growth chamber at25° C., 24 hour dark cycle, 65% relative humidity for 4 days. Theexperiment contained seeds treated with the complex endophyte, inaddition to seed controls (lacking the microbial strains). The number ofseeds that germinated successfully after four days was compared betweenthe endophyte-treated seeds (complex and bacterial) and thenon-endophyte-treated. All treatments were tested in three replicateplates, each containing ten seeds.

Results for the soybean water-stress (drought stress) germination assayare given in Table 5. Complex endophyte treatment improves germinationrate of soybean seedlings under drought (water stressed) conditions vs.formulation controls. Dothideomycetes as complex endophyte hosts appearto impart greater benefit to soybean seedling germination under waterstress (drought stress) conditions vs. their isolated bacterialcomponents, than do Sodariomycetes.

Testing for Germination Enhancement Under Drought Stress (Wheat)

Germination experiments were conducted in 90 mm diameter petri dishesfor wheat. Replicates consisted of a Petri dish, watered with 10 mL ofthe appropriate solution and 20 seeds floating in the solution. Theexperiment contained seeds treated with the complex endophyte, inaddition to seed controls (lacking the microbial strains). To preventlarge variations in Ψ, dishes were sealed with parafilm and the PEGsolutions were renewed weekly by pouring out the existing PEG in thepetri dish and adding the same amount of fresh solution. Petri disheswere maintained in a growth chamber set at 25° C., 16:8 hour light:darkcycle, 70% humidity, and least 120 microE/m{circumflex over ( )}2/slight intensity. The proportion of seeds that germinated successfullyafter three days was compared between the endophyte-treated seeds(complex and bacterial) and the non-endophyte-treated.

Results for the wheat water-stress (drought stress) germination assayare given in Table 6. Complex endophyte treatment, as well as bacterialendophyte treatment, improves germination rate of wheat seedlings underdrought (water stressed) conditions vs. formulation controls.Sodariomycetes as complex endophyte hosts appear to impart greaterbenefit to soybean seedling germination under water stress (droughtstress) conditions vs. their isolated bacterial components, than doDothideomycetes.

Testing for Germination Enhancement in Heat Conditions

Standard germination tests are used to determine if a complex endophyteprotects a seedling or plant against heat stress during germination.Briefly, seeds treated with complex endophytes are placed in between wetbrown paper towels. An equal number of seeds obtained from controlplants that lack the complex endophyte is treated in the same way. Thepaper towels are placed on top of 1×2 ft plastic trays and maintained ina growth chamber set at 16:8 hour light:dark cycle, 70% humidity, and atleast 120 microE/m{circumflex over ( )}2/s light intensity for 7 days. Arange of high temperatures (from 35° C. to 45° C., with increments of 2degrees per assay) is tested to assess the germination of complexendophyte-treated seeds at each temperature. The proportion of seedsthat germinate successfully is compared between the complexendophyte-treated seeds and the non-complex endophyte-treated.

Testing for Germination Enhancement in Cold Conditions

Standard germination tests are used to determine if a complex endophyteprotects a seedling or plant against cold stress during germination.Briefly, seeds treated with complex endophytes are placed in between wetbrown paper towels. An equal number of seeds obtained from controlplants that lack the complex endophyte is treated in the same way. Thepaper towels are placed on top of 1×2 ft plastic trays and maintained ina growth chamber set at 16:8 hour light:dark cycle, 70% humidity, and atleast 120 microE/m{circumflex over ( )}2/s light intensity for 7 days. Arange of low temperatures (from 0° C. to 10° C., with increments of 2degrees per assay) is tested to assess the germination of complexendophyte-treated seeds at each temperature. The proportion of seedsthat germinate successfully is compared between the complexendophyte-treated seeds and the non-complex endophyte-treated.

Testing for Germination Enhancement in High Salt Concentrations

Germination experiments are conducted in 90 mm diameter petri dishes.Replicates consist of a Petri dish, watered with 10 mL of theappropriate solution and 20 seeds floating in the solution. Seedstreated with complex endophytes and seed controls (lacking the microbialstrains) are tested in this way. To prevent large variations in saltconcentration due to evaporation, dishes are sealed with parafilm andthe saline solutions are renewed weekly by pouring out the existingsaline solution in the petri dish and adding the same amount of freshsolution. A range of saline solutions (100-500 mM NaCl) is tested for toassess the germination of complex endophyte-treated seeds at varyingsalt levels. Petri dishes are maintained in a growth chamber set at 25°C., 16:8 hour light:dark cycle, 70% humidity, and at least 120microE/m{circumflex over ( )}2/s light intensity. The proportion ofseeds that germinates successfully after two weeks is compared betweenthe complex endophyte-treated seeds and the non-complexendophyte-treated.

Testing for Germination Enhancement in Soils with High Metal Content

Standard germination tests are used to determine if a complex endophyteprotects a seedling or plant against stress due to high soil metalcontent during germination. Briefly, seeds treated with complexendophytes, are placed in between wet brown paper towels. An equalnumber of seeds obtained from control plants that lack the complexendophyte (complex endophyte-free) is treated in the same way. The papertowels are placed on top of 1×2 ft plastic trays with holes to allowwater drainage. The paper towels are covered with an inch of sterilesand. For each metal to be tested, the sand needs to be treatedappropriately to ensure the release and bioavailability of the metal.For example, in the case of aluminum, the sand is watered with pH 4.0+˜1g/Kg soil Al+3 (−621 microM). The trays are maintained in a growthchamber set at 25° C. and 70% humidity for 7 days. The proportion ofseeds that germinates successfully is compared between the complexendophyte-treated seeds and the non-complex endophyte-treated.

Example 7: Demonstration of Phenotypic Alterations of Host Plants Due toPresence of the Complex Endophyte: Growth Chamber Assays Testing forGrowth Promotion in Growth Chamber in Normal Conditions

Soil is made from a mixture of 60% Sunshine Mix #5 (Sun Gro; Bellevue,Wash., USA) and 40% vermiculite. To determine if a particular complexendophyte is capable of promoting plant growth under normal conditions,pots are prepared in 12-pot no-hole flat trays with 28 grams of dry soilin each pot, and 2 L of filtered water is added to each tray. The wateris allowed to soak into the soil and the soil surface is misted beforeseeding. For each seed-complex endophyte combination, some pots areseeded with 3-5 seeds treated with the complex endophyte and other potsare seeded with 3-5 seeds lacking the complex endophyte (complexendophyte-free plants). The seeded pots are covered with a humidity domeand kept in the dark for 3 days, after which the pots are transferred toa growth chamber set at 25° C., 16:8 hour light:dark cycle, 70%humidity, and at least 120 microE/m{circumflex over ( )}2/s lightintensity. The humidity domes are removed on day 5, or when cotyledonsare fully expanded. After removal of the domes, each pot is irrigated tosaturation with 0.5×Hoagland's solution, then allowing the excesssolution to drain. Seedlings are then thinned to 1 per pot. In thefollowing days, the pots are irrigated to saturation with filteredwater, allowing the excess water to drain after about 30 minutes ofsoaking, and the weight of each 12-pot flat tray is recorded weekly.Canopy area is measured at weekly intervals. Terminal plant height,average leaf area and average leaf length are measured at the end of theflowering stage. The plants are allowed to dry and seed weight ismeasured. Significance of difference in growth between complexendophyte-treated plants and controls lacking the complex endophyte isassessed with the appropriate statistical test depending on thedistribution of the data at p<0.05.

Testing for Growth Promotion in Growth Chamber Under Biotic Stress

Soil is made from a mixture of 60% Sunshine Mix #5 (Sun Gro; Bellevue,Wash., USA) and 40% vermiculite. To determine if a particular complexendophyte is capable of promoting plant growth in the presence of bioticstress, pots are prepared in 12-pot no-hole flat trays with 28 grams ofdry soil in each pot, and 2 L of filtered water is added to each tray.The water is allowed to soak into the soil before planting. For eachseed-complex endophyte combination test, some pots are seeded with 3-5seeds treated with the complex endophyte and other pots are seeded with3-5 seeds lacking the complex endophyte (complex endophyte-free plants).The seeded pots are covered with a humidity dome and kept in the darkfor 3 days, after which the pots are transferred to a growth chamber setat 25° C., 16:8 hour light:dark cycle, 70% humidity, and at least 120μE/m2/s light intensity. The humidity domes are removed on day 5, orwhen cotyledons are fully expanded. After removal of the domes, each potis irrigated to saturation with 0.5×Hoagland's solution, allowing theexcess solution to drain. Seedlings are then thinned to 1 per pot. Inthe following days, the pots are irrigated to saturation with filteredwater, allowing the excess water to drain after about 30 minutes ofsoaking.

Several methods of inoculation are used depending on the lifestyle ofthe pathogen. For leaf pathogens (e.g., Pseudomonas syringeae orColletotrichum graminicola), a suspension of cells for bacteria(10{circumflex over ( )}8 cell/mL) or spores for fungi (10{circumflexover ( )}7 spores/mL) is applied with an applicator on the adaxialsurface of each of the youngest fully expanded leaves. Alternatively forfungal pathogens that do not form conidia easily, two agar plugscontaining mycelium (˜4 mm in diameter) are attached to the adaxialsurface of each of the youngest leaves on each side of the central vein.For vascular pathogens (e.g., Pantoea stewartii or Fusariummoniliforme), the suspension of cells or spores is directly introducedinto the vasculature (5-10 microLiters) through a minor injury inflectedwith a sterile blade. Alternatively, the seedlings can be grownhydroponically in the cell/spore or mycelium suspension. To test theresilience of the plant-complex endophyte combination against insectstresses, such as thrips or aphids, plants are transferred to aspecially-designated growth chamber containing the insects. Soil-borneinsect or nematode pathogens are mixed into or applied topically to thepotting soil. In all cases, care is taken to contain the fungal, insect,nematode or other pathogen and prevent release outside of the immediatetesting area.

The weight of each 12-pot flat tray is recorded weekly. Canopy area ismeasured at weekly intervals. Terminal plant height, average leaf areaand average leaf length are measured at the cease of flowering. Theplants are allowed to dry and seed weight is measured. Significance ofdifference in growth between complex endophyte-treated plants andcontrols lacking the complex endophyte is assessed with the appropriatestatistical test depending on the distribution of the data at p<0.05.

Example 8: Demonstration of Phenotypic Alterations of Host Plants Due toPresence of the Complex Endophyte: Plant Vigor Seedling Assays

Untreated soybean and winter wheat Variety 2 seeds were surfacesterilized using chlorine fumes. Briefly, Erlenmyer flasks containingseeds and a bottle with 100 mL of fresh bleach solution were placed in adesiccation jar located in a fume hood Immediately prior to closing thelid of the desiccation jar, 3 mL hydrochloric acid was carefullypipetted into the bleach. Sterilization was done for 17 hours for soyand 16 hours for wheat. Upon completion the flasks with seeds wereremoved, sealed in sterile foil, and opened in a sterile biosafetycabinet or laminar flow hood for subsequent work.

Complex endophytes and their corresponding endofungal bacteria werecultured in 4 mL PDB using 12-well plates at 25° C. with constantagitation for 5 days and 3 days, respectively. Fungal samples werebriefly sonicated to obtain a homogenous suspension of culture. Surfacesterilized soy and wheat seeds were first coated with 2% sodium alginateto enable microbial adhesion, and then treated with equal volume ofmicrobial culture in a 50 mL Falcon tube. Seeds were mixed forhomogenous coating. Seed treatment calculations were based on 0.01 mLeach of microbial culture and 2% sodium alginate solution for every onegram of seed.

Ten soybean (Variety A) and fifteen wheat (Spring Wheat, Variety 2)treated seeds were placed equidistant to each other on heavy weightgermination paper sandwiches saturated with sterile distilled water foreach treatment. A total of 50 mL water was added to the germinationpaper sandwiches for soy and 25 mL for wheat. The germination papersandwiches were rolled, secured using surgical tape, and placed in twoseparate airtight plastic containers for each crop. Two replicates perSYM treatment were prepared and placed within each container. All stepswere performed under sterile conditions.

All samples were incubated at 24° Celsius with 65% relative humidity indarkness for 4 days to enable seed germination. On day 4, the lid of oneairtight container per crop was removed for the seedlings to allow forgradual water stress and the growth chamber setting was changed to 24°Celsius, 70% relative humidity, 250-300 microEinsten light for 12 hoursfollowed by 18° Celsius, 60% relative humidity for 12 hours of darknessfor 6 days. The second airtight container with seedlings for both cropsremained sealed to maintain plant growth in a non-water stresscondition. Placement of germination rolls was randomized periodically toreduce any positional effect throughout the plant growth period.

At the end of the experiment, each seedling was photographed andmeasured for total root length and mass. Scoring of seedlings were doneby manually measuring each seedling's root and shoot length using eithera ruler or a measurement grid on which the seedlings were placed forimaging. The total mass of seedlings was recorded by weighing allgerminated seedlings within each treatment replicate using an analyticalbalance. Raw data number averages of each treatment were obtained bycomputing mean, standard deviation and standard error for all germinatedseedlings per replicate. Seedlings that failed to germinate or displayedphenotypic abnormalities were excluded from analysis. Data wasrepresented by four plant vigor parameters including root and shootlength, overall plant growth, and total seedling mass. Analyses wereperformed relative to seedlings treated with the formulation control(formulation without complex endophyte or the isolated complex endophytebacterial component).

Wheat Seedling Normal Conditions

Results are shown in Tables 7a-7b.

Plant seedlings grown from seeds treated with complex endophytes orcomplex endophyte bacterial components display a greater average rootlength than do plant seedlings grown from seeds treated with theformulation control. No significant difference was observed in averageroot length between plants grown from seeds treated with complexendophytes vs. isolated bacterial components.

Plant seedlings grown from seeds treated with complex endophytes orcomplex endophyte bacterial components display a greater average shootlength than do plant seedlings grown from seeds treated with theformulation control. Plant seedlings grown from seeds treated withcomplex endophytes display a greater average shoot length than do plantseedlings grown from seeds treated with isolated bacterial components.

Wheat Seedling Drought (Water-Stressed) Conditions

Results are shown in Tables 8a-8b.

Plant seedlings grown from seeds treated with complex endophytes orcomplex endophyte bacterial components display a greater average rootlength than do plant seedlings grown from seeds treated with theformulation control. No significant difference was observed betweenplants grown from seeds treated with complex endophytes vs. isolatedbacterial components.

Plant seedlings grown from seeds treated with complex endophytes orcomplex endophyte bacterial components display a greater average shootlength than do plant seedlings grown from seeds treated with theformulation control. Plant seedlings grown from seeds treated withcomplex endophytes display a greater average shoot length than do plantseedlings grown from seeds treated with isolated bacterial components.

Soy Seedling Normal Conditions

Results are shown in Tables 9a-9b.

Plant seedlings grown from seeds treated with complex endophytes orcomplex endophyte bacterial components display a greater average rootlength than do plant seedlings grown from seeds treated with theformulation control. Plant seedlings grown from seeds treated withcomplex endophytes display a greater average root length than do plantseedlings grown from seeds treated with isolated bacterial components.

Plant seedlings grown from seeds treated with complex endophytes orcomplex endophyte bacterial components display a greater average shootlength than do plant seedlings grown from seeds treated with theformulation control. Plant seedlings grown from seeds treated withisolated bacterial components display a slightly greater average shootlength than do plant seedlings grown from seeds treated with the complexendophytes.

Soy Seedling Drought (Water-Stressed) Conditions

Results are shown in Tables 10a-10b.

Plant seedlings grown from seeds treated with a complex endophyte orcomplex endophyte bacterial component display a greater average rootlength than do plant seedlings grown from seeds treated with theformulation control. Plant seedlings grown from seeds treated withcomplex endophytes display a greater average root length than do plantseedlings grown from seeds treated with isolated bacterial components.

Plant seedlings grown from seeds treated with complex endophytes orcomplex endophyte bacterial components display a greater average shootlength than do plant seedlings grown from seeds treated with theformulation control. No significant difference was observed betweenplants grown from seeds treated with complex endophytes vs. isolatedbacterial components.

Example 9: Demonstration of Phenotypic Alterations of Host Plants Due toPresence of the Complex Endophyte: Greenhouse Assessments

Seeds were coated with complex endophytes and isolated bacterialendophytes as follows. 2% sodium alginate (SA) was prepared andautoclaved. An Erlenmeyer flask was filled with appropriate amount ofdeionized water and warmed to about 50 degrees on a heat plate withagitation using stirring bar. SA powder was poured slowly until it alldissolved. The solution was autoclaved at 121° C. @ 15 PSI for 30minutes.

Talcum powder was autoclaved in a dry cycle (121° C. @ 15 PSI for 30minutes) and aliquoted in Ziploc bags or 50 ml falcon tubes.

Microbial (complex endophyte or fungal endophyte) inocula were preparedin the amounts indicated below. For controls, fungal powder wassubstituted with talc, or liquid fungus with the liquid medium (YeastExtract Peptone Broth), respectively.

For wheat fungal powder seed treatment, seeds were placed in a largeplastic container. 50 mL of the 2% SA was applied per kilogram of seedsto be treated. The container was covered with a hinged lid and shakenslowly in orbital motion for about 20 seconds to disperse the SA. 12.5 gof fungal powder was premixed with 137.5 g of talcum powder, per kg ofseed to be treated. A mixture of the fungal inocula and talc wasdispersed evenly on top of the seeds, the container covered, and theseeds shaken slowly in orbital motion for about 20 seconds. Excesspowder was sieved off and the seeds packed in paper bags for storageprior to planting.

For wheat fungal liquid seed treatment, seeds were placed in a largeplastic container. 25 ml of 2% SA per kg of seed and the same amount offungal culture (25 ml per kg of seed) was poured on the seeds. Thecontainer was covered with a hinged lid and shaken slowly in orbitalmotion for about 20 seconds to disperse the SA. 137.5 g of talcum powderper kg of seed was added and dispersed evenly, the container covered,and the seeds shaken slowly in orbital motion for about 20 seconds.Excess formulation was sieved off and the seeds packed in paper bags forstorage prior to planting.

For each treatment, a standard greenhouse flat divided into 8compartments with a standard 801 insert was filled with Fafard blendsoil (900 mL per compartment) and allowed to soak in 2 L water toprovide normal soil moisture conditions. 12 seeds of 2 winter wheatvarieties were planted in each compartment at a consistent depth of 2cm. Pots were watered approximately 2-4 hours prior to planting seeds.The number of seeds planted per pot depends on the type of crop. Forexample, three seeds can be planted for soy, four for wheat, and one forcorn. Plants are grown at a 21° C./18° C. day/night regime with a 14hour photoperiod at a light intensity of 800 microE/m{circumflex over( )}2/s and 40% relative humidity.

Drought experiments were performed as described in the art. For example,water was withheld until the plants start wilting, were watered again,then allowed to enter into another drought cycle. The drought cycleswere continued until the plant reached maturity.

Plants grown from seeds treated with the complex endophyte SYM166 weretested alongside plants grown from seeds treated with a controlformulation (formulation minus endophyte) as well as plants grown fromseeds treated control fungal endophytes that are not known to be complexendophytes and are of different genera than SYM166.

Emergence of germinated seeds was observed from days 3 to 8 afterplanting. Seedlings were harvested at day 8 after planting and driedovernight in a convection oven to collect dry weight and height of eachseedling's aerial parts.

As shown in FIG. 2, the complex endophyte SYM166 demonstrated improvedemergence rates in greenhouse wheat plants, versus plants treated withformulation control or fungal endophytes that were not complex. Inparticular, the complex endophyte appears to improve the early phases ofemergence, as demonstrated by improved emergence in Days 3, 4, and 5.

A shown in FIG. 3, the complex endophyte SYM166 demonstrated greaterbenefit to greenhouse wheat plants with respect to shoot biomass, versusplants treated with formulation control or fungal endophytes that werenot complex.

Example 10: Demonstration of Phenotypic Alterations of Host Plants Dueto Presence of the Complex Endophyte: Field Trials

Winter wheat seed untreated seed was coated with a specific formulationdepending on the type of strain, and a formulation control lacking theendophyte was included for each type of formulation. For strainsformulated as dry powders (e.g., SYM166, a.k.a. SYM16670; e.g., fungalendophytes that are not known to be complex endophytes and are ofdifferent genera as SYM166, as controls), 2% sodium alginate (16.6 mLper kg seed) was applied and the seeds were agitated for 20 s todisperse the sticker. Then a 1:1 mixture of powder and talc (15 g fungalpowder per kg seed) was applied and the seeds are agitated for 20 s todisperse the powder. Then FloRite (13.1 mL per kg seed) was applied andseeds were agitated for 20 s to disperse the flowability polymer.

Treated seeds were placed in paper bags and allowed to dry overnight ina well ventilated space before planting.

All fields (2% slopes) were fallow for the previous season, treated withglyphosate pre-planting and managed with conventional tillage.Untreated, formulation-treated and endophyte-treated seeds were drilledin with a plot planter in a randomized complete block design in plots of7 by 40 ft with 7 rows on 7 in spacing. Seeding rate was 60 lbs per acreand planting depth was 0.5 in. Five interior rows were harvested with aHege 135 B plot combine for yield assessment with the outer rows used asa buffer between plots. Grain yield (lb per plot), test weight (lb perbushel) and moisture (%) were taken directly on the combine. Yield drybushels per acre was calculated using per plot test weights andnormalized for a grain storage moisture of 13%. Thousand kernel seedweight (TKW g) was established per plot.

Early and mid-season metrics were collected. Emergence counts were takenover 10 feet on two interior rows at a timepoint when the control plotsreached 50% emergence and this area was marked for the harvestable headcount at the end of the season. A visual assessment of seedling vigor(1-10 rating scale) was taken at emergence. Tillers were counted on 5individual plants at 30 days after seeding (DAS) both pre- andpost-vernalization. A phytotoxicity visual assessment (%) was taken onthe same plants used for tiller counts. Directly prior to harvest,harvestable heads were quantified over a square yard.

Yield (wet and dry, per acre) results for winter wheat seeds grown underdryland (non-irrigated) conditions and treated with complex endophyteSYM166 are given in Table 11, compared to winter wheat seeds treatedwith non-complex fungal endophytes as well as fungal formulationcontrols. Winter wheat grown from seeds treated with complex endophyteSYM166 demonstrate improved yield (both wet bushels per acre and drybushels per acre) compared to seeds treated with either the fungalformulation control or with non-complex fungal endophytes.

Yield (wet and dry, per acre) results for spring wheat seeds grown underdryland (non-irrigated) conditions and treated with complex endophyteSYM166 are given in Table 12, compared to winter wheat seeds treatedwith non-complex fungal endophytes as well as fungal formulationcontrols. Spring wheat grown from seeds treated with complex endophyteSYM166 demonstrate improved yield (both wet bushels per acre and drybushels per acre) compared to seeds treated with either the fungalformulation control or with non-complex fungal endophytes.

Example 11: Demonstration of Improved Survivability of BacteriaAssociated with Plant Elements, when Said Bacteria are Encapsulatedwithin a Host Fungus

This example describes the methods and results for demonstrating thatbacteria encompassed within a host fungus display greater survivabilityon treated seeds than does the identical bacterial strain isolated andtreated on seeds.

Corn seeds were associated with individual microbial (endofungal complexendophyte and endofungal bacterial endophyte) cultures as follows.Untreated organic corn seeds were surface sterilized using chlorinefumes. Briefly, Erlenmyer flasks containing seeds and a bottle with 100mL of fresh bleach solution were placed in a desiccation jar located ina fume hood Immediately prior to closing the lid of the desiccation jar,3 mL hydrochloric acid was carefully pipetted into the bleach.Sterilization was done for 14 hours, and upon completion the flasks withseeds were removed, sealed in sterile foil, and opened in a sterilebiosafety cabinet or laminar flow hood for subsequent work. Surfacesterilized organic corn seeds were first coated with 2% sodium alginateto enable microbial adhesion, and then treated with equal volumes of theappropriate microbial culture in a 50 mL Falcon tube. Seeds were mixedfor homogenous coating. Seed treatment calculations were based on 23 mLeach of microbial culture and 2% sodium alginate solution for every onekilogram of seed.

All steps of this method were performed under sterile conditions.Complex endophytes (host fungi comprising component bacteria) were grownin cultures in 150 mL of full strength Potato Dextrose Broth (PDB) at 24grams per liter, in Erlenmyer flasks for 7 days at 25 degrees Celsiuswith constant agitation (130 RPM).

Endofungal bacteria were isolated from host fungi by plating the complexendohytes onto cycloheximide Lysogeny Broth (LB) plates. Cycloheximideis an antifungal agent that kills the host fungus, allowing thecomponent bacteria to grow alone. SYM166 was grown in full strengthPotato Dextrose Broth (PDB) at 24 grams per liter for 5 days. 20 mL fromthe growth medium was extracted and sonicated to homogenize, and platedin serial dilutions of 1:10, 1:100, and 1:1000. 500 microliters of eachdilution was plated in duplicated LB plates with cycloheximide (at 50micrograms per milliliter). Bacterial colonies were counted and isolatedfrom the serial dilution plates. Pure isolates of the endofungalbacteria were grown as lawns in LB for 1 day.

All results are summarized in FIG. 4. The complex endophyte SYM166demonstrated a greater than 2 fold survivability at Day 1 post seedtreatment, and a 16 fold improvement in bacterial survivability versusthe bacterial endophyte alone at Day 36 post seed treatment.

Example 11: Demonstration of Improved Bacterial Tolerance toEnvironmental Stresses when Encapsulated within a Host Fungus

All Bacteria can be sensitive to molecules in the environment, such asantibiotics. The inventors herein developed a method of demonstratingimproved tolerance of bacteria to antibiotics, when said bacteria areencapsulated within a host fungus.

Known endofungal endophyte SYM15779, comprising the bacterium EHB15779,was treated with gentamicin, and compared to a control culture ofSYM15779 not treated with gentamicin.

Fungal mycelia were washed using 1 mL 10 mM MgCl₂ twice in microfugetubes. Samples were centrifuged at 16,110 RPM at room temperature for 3minutes and the solution decanted. The residual solution was pipettedout. Samples were incubated in either 0.05 mg/mL or 0.075 mg/mLGentamicin, prepared with 50 mM Phosphate Saline Buffer, pH 7.0 for 1hour. 0.2 mL solution was determined to be sufficient.

DNase I cocktail was prepared by the addition of 5 μL of DNase I and 5μL 10× DNAse Buffer (DNAse I cocktail) per treatment. When five sampleswere being treated, a microfuge tube of 25 μL (5×5 μL) of each solutionwas prepared. Solutions were stored in the refrigerator (4° C.) untiluse.

Following incubation in the antibiotic solution, the solution wasdecanted. A minimum of 0.1 mL MgCl₂ per tube was added to thoroughlyimmerse the sample, and 10 μL of the DNAse I cocktail was immediatelyadded for each sample. Samples were incubated for 15 minutes.

Proteinase K (10 mg/mL final concentration) in 10 mM MgCl₂ (Proteinase Kcocktail) was prepared, in enough volume to add 0.2 mL/sample.

DNAse I solution was removed from the tubes after incubation time, viadecanting or pipetting.

Proteinase K wash was conducted by adding at least 0.2 mL of theProteinase K cocktail/sample and the samples were incubated for 15minutes.

The Proteinase K solution was then pipetted out.

Samples were washed thoroughly 8 to 10 times with 10 mM MgCl₂ bypipetting up and down the solution during the procedure, and ensuringthat all outer parts of the mycelia were being thoroughly washed.

Samples were stored in the refrigerator at 4° C. until the genomic DNAextraction of fungi was performed, followed by PCR amplification of thebacterial gene relative to control samples.

Presence or absence of bacteria in the washed fungal samples wasverified by PCR using 16S rRNA gene amplification, alongsideexperimental control samples consisting of: (1) control samples of aknown native endofungus that is washed the same way to ensure thewashing does not strip away internal bacterium, (2) control samples of aknown native endofungus that is untreated, and (3) untreated sample of aknown non-complex endophyte fungus (fungus not known to comprise acomponent bacterium, SYM15890) with about 0.1 mL of pure bacterialculture at log phase added on the surface and washed the same way. PCRresults were also compared to that of a control isolated bacterium.

Results are show in FIG. 5. The 16S bacterial identification sequencewas detected for the control bacterium, SYM15779 before and after thegentamicin treatment and washings described in this example, as well inas the non-complex endophyte fungus SYM15890 that was spiked with thepure bacterial culture, after the gentamicin treatment and washingsdescribed in this example. The 16S bacterial identification sequence wasnot detected in the sample comprising non-complex endophyte fungusSYM15890 after the gentamicin treatment and washings described in thisexample

Viability of the endofungal bacterium EHB15779 after gentamicintreatment and wash was confirmed in culture post-treatment: theendofungal bacteria continued to grow and was observed to come out ofthe fungal hyphae.

While the invention has been particularly shown and described withreference to a preferred embodiment and various alternate embodiments,it will be understood by persons skilled in the relevant art thatvarious changes in form and details can be made therein withoutdeparting from the spirit and scope of the invention.

All references, issued patents, and patent applications cited within thebody of the instant specification are hereby incorporated by referencein their entirety, for all purposes.

TABLE 1 Bacterial endofungal endophytes of the present invention SEQ IDKingdom Phylum Class Order Family Genus 1 Bacteria Firmicutes BacilliBacillales Bacillaceae Bacillus 2 Bacteria Firmicutes Bacilli BacillalesBacillaceae Bacillus 3 Bacteria Firmicutes Bacilli BacillalesBacillaceae Bacillus 4 Bacteria Firmicutes Bacilli BacillalesPaenibacillaceae Paenibacillus 5 Bacteria Firmicutes Bacilli BacillalesPaenibacillaceae Paenibacillus 6 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Moraxellaceae Acinetobacter 7Bacteria Proteobacteria Betaproteobacteria BurkholderialesBurkholderiaceae Burkholderia 8 Bacteria ProteobacteriaAlphaproteobacteria Sphingomonadales Sphingomonadaceae Sphingomonas 9Bacteria Proteobacteria Gammaproteobacteria XanthomonadalesXanthomonadaceae Luteibacter 10 Bacteria ProteobacteriaAlphaproteobacteria Sphingomonadales Sphingomonadaceae Sphingomonas 11Bacteria Firmicutes Bacilli Bacillales Paenibacillaceae Paenibacillus 12Bacteria Firmicutes Bacilli Bacillales Paenibacillaceae Paenibacillus 13Bacteria Firmicutes Bacilli Bacillales Paenibacillaceae Paenibacillus 14Bacteria Proteobacteria Betaproteobacteria BurkholderialesBurkholderiaceae Ralstonia 15 Bacteria Firmicutes Bacilli BacillalesBacillaceae Bacillus 16 Bacteria Proteobacteria BetaproteobacteriaBurkholderiales Burkholderiaceae Ralstonia 17 Bacteria FirmicutesBacilli Bacillales Paenibacillaceae Paenibacillus 18 Bacteria FirmicutesBacilli Bacillales Paenibacillaceae Paenibacillus 19 Bacteria FirmicutesBacilli Bacillales Paenibacillaceae Paenibacillus 20 Bacteria FirmicutesBacilli Bacillales Bacillaceae Bacillus 21 Bacteria Firmicutes BacilliBacillales Paenibacillaceae Paenibacillus 22 Bacteria Firmicutes BacilliBacillales Paenibacillaceae Paenibacillus 23 Bacteria Firmicutes BacilliBacillales Paenibacillaceae Paenibacillus 24 Bacteria Firmicutes BacilliBacillales Paenibacillaceae Paenibacillus 25 Bacteria Firmicutes BacilliBacillales Paenibacillaceae Paenibacillus 26 Bacteria Firmicutes BacilliBacillales Paenibacillaceae Paenibacillus 27 Bacteria ProteobacteriaBetaproteobacteria Burkholderiales Oxalobacteraceae Massilia 28 BacteriaProteobacteria Betaproteobacteria Burkholderiales OxalobacteraceaeMassilia 29 Bacteria Proteobacteria Betaproteobacteria BurkholderialesBurkholderiaceae Ralstonia 30 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Moraxellaceae Acinetobacter 31Bacteria Proteobacteria Gammaproteobacteria XanthomonadalesXanthomonadaceae Luteibacter 32 Bacteria ProteobacteriaBetaproteobacteria Burkholderiales Comamonadaceae Variovorax 33 BacteriaProteobacteria Betaproteobacteria Burkholderiales BurkholderiaceaeRalstonia 34 Bacteria Firmicutes Bacilli Bacillales Bacillaceae Bacillus35 Bacteria Firmicutes Bacilli Bacillales Bacillaceae Bacillus 36Bacteria Firmicutes Bacilli Bacillales Paenibacillaceae Paenibacillus 37Bacteria Firmicutes Bacilli Bacillales Paenibacillaceae Paenibacillus 38Bacteria Proteobacteria Betaproteobacteria BurkholderialesBurkholderiaceae Burkholderia 39 Bacteria Firmicutes Bacilli BacillalesBacillaceae Bacillus 40 Bacteria Proteobacteria GammaproteobacteriaXanthomonadales Xanthomonadaceae Luteibacter 41 Bacteria ProteobacteriaBetaproteobacteria Burkholderiales Burkholderiaceae Ralstonia 42Bacteria Firmicutes Bacilli Bacillales Bacillaceae Bacillus 43 BacteriaActinobacteria Actinobacteria Actinomycetales MicrobacteriaceaeCurtobacterium 44 Bacteria Actinobacteria Actinobacteria ActinomycetalesMicrobacteriaceae Curtobacterium 45 Bacteria ProteobacteriaGammaproteobacteria Xanthomonadales Xanthomonadaceae Luteibacter 46Bacteria Proteobacteria Gammaproteobacteria XanthomonadalesXanthomonadaceae Luteibacter 47 Bacteria ProteobacteriaGammaproteobacteria Enterobacteriales Enterobacteriaceae Pantoea 48Bacteria Proteobacteria Gammaproteobacteria XanthomonadalesXanthomonadaceae Luteibacter 49 Bacteria Firmicutes Bacilli BacillalesBacillaceae Bacillus 50 Bacteria Firmicutes Bacilli BacillalesBacillaceae Bacillus 51 Bacteria Firmicutes Bacilli BacillalesPaenibacillaceae Paenibacillus 52 Bacteria Firmicutes Bacilli BacillalesPaenibacillaceae Paenibacillus 53 Bacteria Firmicutes Bacilli BacillalesBacillaceae Bacillus 54 Bacteria Firmicutes Bacilli BacillalesBacillaceae Bacillus 55 Bacteria Proteobacteria GammaproteobacteriaEnterobacteriales Enterobacteriaceae Pantoea 56 Bacteria ProteobacteriaAlphaproteobacteria Rhizobiales Rhizobiaceae Rhizobium 57 BacteriaProteobacteria Gammaproteobacteria Enterobacteriales EnterobacteriaceaePantoea 58 Bacteria Proteobacteria Gammaproteobacteria XanthomonadalesXanthomonadaceae Luteibacter 59 Bacteria ProteobacteriaGammaproteobacteria Xanthomonadales Xanthomonadaceae Luteibacter 60Bacteria Proteobacteria Gammaproteobacteria XanthomonadalesXanthomonadaceae Luteibacter 61 Bacteria ProteobacteriaGammaproteobacteria Xanthomonadales Xanthomonadaceae Luteibacter 62Bacteria Proteobacteria Gammaproteobacteria EnterobacterialesEnterobacteriaceae Erwinia 63 Bacteria ProteobacteriaGammaproteobacteria Xanthomonadales Xanthomonadaceae Luteibacter 64Bacteria Proteobacteria Gammaproteobacteria XanthomonadalesXanthomonadaceae Luteibacter 65 Bacteria ProteobacteriaGammaproteobacteria Xanthomonadales Xanthomonadaceae Luteibacter 66Bacteria Proteobacteria Gammaproteobacteria XanthomonadalesXanthomonadaceae Luteibacter 67 Bacteria ProteobacteriaGammaproteobacteria Xanthomonadales Xanthomonadaceae Luteibacter 68Bacteria Proteobacteria Gammaproteobacteria XanthomonadalesXanthomonadaceae Luteibacter 69 Bacteria ProteobacteriaGammaproteobacteria Enterobacteriales Enterobacteriaceae Erwinia 70Bacteria Proteobacteria Betaproteobacteria BurkholderialesBurkholderiaceae Ralstonia 71 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Pseudomonadaceae Pseudomonas 72Bacteria Proteobacteria Alphaproteobacteria CaulobacteralesCaulobacteraceae Caulobacter 73 Bacteria ProteobacteriaAlphaproteobacteria Caulobacterales Caulobacteraceae Caulobacter 74Bacteria Proteobacteria Gammaproteobacteria PseudomonadalesPseudomonadaceae Pseudomonas 75 Bacteria ProteobacteriaGammaproteobacteria Xanthomonadales Xanthomonadaceae Stenotrophomonas 76Bacteria Proteobacteria Gammaproteobacteria PseudomonadalesPseudomonadaceae Pseudomonas 77 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Pseudomonadaceae Pseudomonas 78Bacteria Bacteroidetes Cytophagia Cytophagales CytophagaceaeHymenobacter 79 Bacteria Proteobacteria GammaproteobacteriaPseudomonadales Pseudomonadaceae Pseudomonas 80 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Pseudomonadaceae Pseudomonas 81Bacteria Proteobacteria Gammaproteobacteria PseudomonadalesPseudomonadaceae Pseudomonas 82 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Pseudomonadaceae Pseudomonas 83Bacteria Proteobacteria Gammaproteobacteria PseudomonadalesPseudomonadaceae Pseudomonas 84 Bacteria ProteobacteriaBetaproteobacteria Burkholderiales Comamonadaceae Pelomonas 85 BacteriaProteobacteria Alphaproteobacteria Sphingomonadales SphingomonadaceaeSphingomonas 86 Bacteria Proteobacteria GammaproteobacteriaPseudomonadales Pseudomonadaceae Pseudomonas 87 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Pseudomonadaceae Pseudomonas 88Bacteria Proteobacteria Gammaproteobacteria PseudomonadalesPseudomonadaceae Pseudomonas 89 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Pseudomonadaceae Pseudomonas 90Bacteria Proteobacteria Gammaproteobacteria PseudomonadalesPseudomonadaceae Pseudomonas 91 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Pseudomonadaceae Pseudomonas 92Bacteria Proteobacteria Gammaproteobacteria PseudomonadalesPseudomonadaceae Pseudomonas 93 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Pseudomonadaceae Pseudomonas 94Bacteria Proteobacteria Gammaproteobacteria PseudomonadalesPseudomonadaceae Pseudomonas 95 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Pseudomonadaceae Pseudomonas 96Bacteria Proteobacteria Alphaproteobacteria SphingomonadalesSphingomonadaceae Sphingomonas 97 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Pseudomonadaceae Pseudomonas 98Bacteria Proteobacteria Gammaproteobacteria PseudomonadalesPseudomonadaceae Pseudomonas 99 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Pseudomonadaceae Pseudomonas 100Bacteria Proteobacteria Gammaproteobacteria PseudomonadalesPseudomonadaceae Pseudomonas 101 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Pseudomonadaceae Pseudomonas 102Bacteria Proteobacteria Gammaproteobacteria PseudomonadalesPseudomonadaceae Pseudomonas 103 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Pseudomonadaceae Pseudomonas 104Bacteria Proteobacteria Gammaproteobacteria PseudomonadalesPseudomonadaceae Pseudomonas 105 Bacteria Actinobacteria ActinobacteriaActinomycetales Nocardiaceae Rhodococcus 106 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Moraxellaceae Enhydrobacter 107Bacteria Proteobacteria Gammaproteobacteria PseudomonadalesMoraxellaceae Enhydrobacter 108 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Moraxellaceae Perlucidibaca 109Bacteria Proteobacteria Gammaproteobacteria XanthomonadalesXanthomonadaceae Dyella 110 Bacteria Proteobacteria GammaproteobacteriaEnterobacteriales Enterobacteriaceae Escherichia/Shigella 111 BacteriaProteobacteria Betaproteobacteria Burkholderiales Comamonadaceae Delftia112 Bacteria Proteobacteria Alphaproteobacteria RhizobialesBradyrhizobiaceae Oligotropha 113 Bacteria Actinobacteria ActinobacteriaActinomycetales Microbacteriaceae Microbacterium 114 BacteriaProteobacteria Betaproteobacteria Burkholderiales OxalobacteraceaeMassilia 115 Bacteria Actinobacteria Actinobacteria ActinomycetalesPropionibacteriaceae Propionibacterium 116 Bacteria ActinobacteriaActinobacteria Actinomycetales Microbacteriaceae Okibacterium 117Bacteria Actinobacteria Actinobacteria Actinomycetales MicrobacteriaceaeMicrobacterium 118 Bacteria Actinobacteria ActinobacteriaActinomycetales Microbacteriaceae Microbacterium 119 BacteriaActinobacteria Actinobacteria Actinomycetales MicrobacteriaceaeMicrobacterium 120 Bacteria Bacteroidetes FlavobacteriiaFlavobacteriales Flavobacteriaceae Chryseobacterium 121 BacteriaProteobacteria Betaproteobacteria Burkholderiales OxalobacteraceaeHerbaspirillum 122 Bacteria Bacteroidetes FlavobacteriiaFlavobacteriales Flavobacteriaceae Chryseobacterium 123 BacteriaProteobacteria Alphaproteobacteria Rhizobiales Rhizobiaceae Rhizobium124 Bacteria Proteobacteria Alphaproteobacteria RhizobialesPhyllobacteriaceae Mesorhizobium 125 Bacteria ProteobacteriaAlphaproteobacteria Rhizobiales Bradyrhizobiaceae Rhodopseudomonas 126Bacteria Proteobacteria Betaproteobacteria BurkholderialesBurkholderiaceae Burkholderia 127 Bacteria ProteobacteriaBetaproteobacteria Burkholderiales Oxalobacteraceae Herbaspirillum 128Archaea Crenarchaeota Thermoprotei Sulfolobales SulfolobaceaeSulfurisphaera 129 Bacteria Proteobacteria GammaproteobacteriaEnterobacteriales Enterobacteriaceae Kosakonia 130 BacteriaActinobacteria Actinobacteria Actinomycetales StreptomycetaceaeStreptomyces 131 Bacteria Fusobacteria Fusobacteriia FusobacterialesLeptotrichiaceae Sebaldella 132 Bacteria Actinobacteria ActinobacteriaActinomycetales Microbacteriaceae Curtobacterium 133 BacteriaProteobacteria Gammaproteobacteria Pseudomonadales MoraxellaceaeEnhydrobacter 134 Bacteria Proteobacteria AlphaproteobacteriaSphingomonadales Sphingomonadaceae Sphingomonas 135 BacteriaProteobacteria Alphaproteobacteria Sphingomonadales SphingomonadaceaeSphingomonas 136 Bacteria Actinobacteria Actinobacteria ActinomycetalesMicromonosporaceae Actinoplanes 137 Bacteria ProteobacteriaAlphaproteobacteria Rhizobiales Beijerinckiaceae Beijerinckia 138Bacteria Proteobacteria Gammaproteobacteria EnterobacterialesEnterobacteriaceae Erwinia 139 Bacteria ProteobacteriaAlphaproteobacteria Rhizobiales Bradyrhizobiaceae Bradyrhizobium 140Bacteria Proteobacteria Alphaproteobacteria RhizobialesBradyrhizobiaceae Bradyrhizobium 141 Bacteria ProteobacteriaAlphaproteobacteria Rhizobiales Bradyrhizobiaceae Bradyrhizobium 142Bacteria Proteobacteria Alphaproteobacteria RhizobialesBradyrhizobiaceae Bradyrhizobium 143 Bacteria ProteobacteriaAlphaproteobacteria Rhizobiales Bradyrhizobiaceae Bradyrhizobium 144Bacteria Proteobacteria Alphaproteobacteria RhizobialesBradyrhizobiaceae Bradyrhizobium 145 Bacteria ProteobacteriaAlphaproteobacteria Rhizobiales Bradyrhizobiaceae Bradyrhizobium 146Bacteria Proteobacteria Alphaproteobacteria RhizobialesBradyrhizobiaceae Bradyrhizobium 147 Bacteria ActinobacteriaActinobacteria Actinomycetales Intrasporangiaceae Oryzihumus 148Bacteria Actinobacteria Actinobacteria CoriobacterialesCoriobacteriaceae Adlercreutzia 149 Bacteria ProteobacteriaBetaproteobacteria Burkholderiales Comamonadaceae Variovorax 150Bacteria Proteobacteria Alphaproteobacteria RhizobialesPhyllobacteriaceae Mesorhizobium 151 Bacteria Firmicutes BacilliBacillales Incertae Sedis XII Exiguobacterium 152 Bacteria FirmicutesBacilli Bacillales Incertae Sedis XII Exiguobacterium 153 BacteriaActinobacteria Actinobacteria Actinomycetales incertae_sedisSinosporangium 154 Bacteria Firmicutes Bacilli BacillalesStaphylococcaceae Staphylococcus 155 Bacteria Firmicutes BacilliBacillales Staphylococcaceae Staphylococcus 156 Bacteria ActinobacteriaActinobacteria Actinomycetales incertae_sedis Sinosporangium 157Bacteria Firmicutes Bacilli Bacillales Bacillaceae Bacillus 158 BacteriaFirmicutes Bacilli Bacillales Bacillaceae Bacillus 159 BacteriaProteobacteria Betaproteobacteria Burkholderiales ComamonadaceaeVariovorax 160 Bacteria Proteobacteria BetaproteobacteriaBurkholderiales Comamonadaceae Variovorax 161 Archaea CrenarchaeotaThermoprotei Sulfolobales Sulfolobaceae Stygiolobus 162 BacteriaProteobacteria Betaproteobacteria Burkholderiales ComamonadaceaeVariovorax 163 Bacteria Proteobacteria Alphaproteobacteria RhizobialesBradyrhizobiaceae Bradyrhizobium 164 Bacteria ProteobacteriaAlphaproteobacteria Rhizobiales Bradyrhizobiaceae Bradyrhizobium 165Bacteria Firmicutes Bacilli Lactobacillales CarnobacteriaceaeAtopostipes 166 Bacteria Firmicutes Bacilli LactobacillalesCarnobacteriaceae Atopostipes 167 Bacteria ProteobacteriaGammaproteobacteria Enterobacteriales Enterobacteriaceae Serratia 168Bacteria Proteobacteria Gammaproteobacteria EnterobacterialesEnterobacteriaceae Serratia 169 Archaea Crenarchaeota ThermoproteiSulfolobales Sulfolobaceae Sulfurisphaera 170 Bacteria VerrucomicrobiaOpitutae Puniceicoccales Puniceicoccaceae Coraliomargarita 171 BacteriaProteobacteria Gammaproteobacteria Enterobacteriales EnterobacteriaceaeEnterobacter 172 Bacteria Proteobacteria GammaproteobacteriaEnterobacteriales Enterobacteriaceae Serratia 173 Archaea EuryarchaeotaHalobacteria Halobacteriales Halobacteriaceae Halobaculum 174 ArchaeaEuryarchaeota Halobacteria Halobacteriales Halobacteriaceae Halosimplex175 Bacteria Proteobacteria Gammaproteobacteria XanthomonadalesXanthomonadaceae Luteibacter 176 Bacteria ProteobacteriaGammaproteobacteria Xanthomonadales Xanthomonadaceae Luteibacter 177Bacteria Actinobacteria Actinobacteria Actinomycetales MicrobacteriaceaePseudoclavibacter 178 Bacteria Actinobacteria ActinobacteriaActinomycetales Microbacteriaceae Zimmermannella 179 BacteriaProteobacteria Gammaproteobacteria Enterobacteriales EnterobacteriaceaeSerratia 180 Bacteria Proteobacteria GammaproteobacteriaEnterobacteriales Enterobacteriaceae Serratia 181 BacteriaProteobacteria Gammaproteobacteria Enterobacteriales EnterobacteriaceaeSerratia 182 Bacteria Proteobacteria GammaproteobacteriaEnterobacteriales Enterobacteriaceae Serratia 183 BacteriaProteobacteria Gammaproteobacteria Enterobacteriales EnterobacteriaceaeSerratia 184 Bacteria Proteobacteria GammaproteobacteriaEnterobacteriales Enterobacteriaceae Serratia 185 BacteriaProteobacteria Gammaproteobacteria Enterobacteriales EnterobacteriaceaeSerratia 186 Bacteria Proteobacteria GammaproteobacteriaEnterobacteriales Enterobacteriaceae Serratia 187 BacteriaProteobacteria Gammaproteobacteria Enterobacteriales EnterobacteriaceaeSerratia 188 Bacteria Proteobacteria GammaproteobacteriaEnterobacteriales Enterobacteriaceae Serratia 189 BacteriaProteobacteria Gammaproteobacteria Enterobacteriales EnterobacteriaceaeSerratia 190 Bacteria Proteobacteria Betaproteobacteria BurkholderialesComamonadaceae Variovorax 191 Bacteria Proteobacteria BetaproteobacteriaBurkholderiales Comamonadaceae Variovorax 192 Bacteria FirmicutesBacilli Bacillales Bacillaceae Bacillus 193 Archaea NanohaloarchaeotaNanohaloarchaea Incertae sedis Incertae sedis Candidatus Haloredivivus194 Archaea Euryarchaeota Archaeoglobi Archaeoglobales ArchaeoglobaceaeFerroglobus 195 Bacteria Proteobacteria GammaproteobacteriaXanthomonadales Xanthomonadaceae Luteibacter 196 Bacteria ProteobacteriaGammaproteobacteria Xanthomonadales Xanthomonadaceae Luteibacter 197Archaea Nanohaloarchaeota Nanohaloarchaea Incertae sedis Incertae sedisCandidatus Haloredivivus 198 Archaea Euryarchaeota ArchaeoglobiArchaeoglobales Archaeoglobaceae Ferroglobus 199 Bacteria ActinobacteriaActinobacteria Actinomycetales Propionibacteriaceae Propionibacterium200 Bacteria Proteobacteria Alphaproteobacteria RhizobialesBradyrhizobiaceae Bradyrhizobium 201 Bacteria ProteobacteriaAlphaproteobacteria Rhizobiales Bradyrhizobiaceae Bradyrhizobium 202Bacteria Firmicutes Bacilli Lactobacillales StreptococcaceaeStreptococcus 203 Bacteria Firmicutes Bacilli LactobacillalesStreptococcaceae Streptococcus 204 Bacteria Firmicutes BacilliLactobacillales Streptococcaceae Streptococcus 205 Bacteria FirmicutesBacilli Lactobacillales Streptococcaceae Streptococcus 206 Bacteriacandidate division Incertae sedis Incertae sedis Incertae sedisWPS-2_genera_incertae_sedis WPS-2 207 Bacteria ProteobacteriaAlphaproteobacteria Rhizobiales Bradyrhizobiaceae Afipia 208 BacteriaProteobacteria Alphaproteobacteria Rhizobiales BradyrhizobiaceaeRhodopseudomonas 209 Bacteria Firmicutes Bacilli LactobacillalesStreptococcaceae Streptococcus 210 Bacteria Firmicutes BacilliLactobacillales Streptococcaceae Streptococcus 211 BacteriaCyanobacteria Incertae sedis Incertae sedis Incertae sedis Incertaesedis 212 Bacteria Cyanobacteria Incertae sedis Incertae sedis Incertaesedis Incertae sedis 213 Bacteria Proteobacteria GammaproteobacteriaPseudomonadales Pseudomonadaceae Pseudomonas 214 Bacteria ProteobacteriaGammaproteobacteria Pseudomonadales Pseudomonadaceae Pseudomonas 215Bacteria Firmicutes Bacilli Lactobacillales LactobacillaceaeLactobacillus 216 Bacteria Firmicutes Bacilli LactobacillalesLactobacillaceae Lactobacillus 217 Bacteria Cyanobacteria Incertae sedisIncertae sedis Incertae sedis Incertae sedis 218 Bacteria CyanobacteriaIncertae sedis Incertae sedis Incertae sedis Incertae sedis 219 BacteriaFirmicutes Bacilli Lactobacillales Streptococcaceae Streptococcus 220Bacteria Firmicutes Bacilli Lactobacillales StreptococcaceaeStreptococcus 221 Bacteria Proteobacteria AlphaproteobacteriaRhizobiales Rhizobiaceae Rhizobium 222 Bacteria ProteobacteriaAlphaproteobacteria Rhizobiales Rhizobiaceae Rhizobium 223 BacteriaProteobacteria Alphaproteobacteria Rhizobiales Rhizobiaceae Rhizobium224 Bacteria Proteobacteria Alphaproteobacteria Rhizobiales RhizobiaceaeRhizobium 225 Bacteria Firmicutes Bacilli LactobacillalesStreptococcaceae Streptococcus 226 Bacteria Firmicutes BacilliLactobacillales Streptococcaceae Streptococcus 227 BacteriaProteobacteria Alphaproteobacteria Rhizobiales BradyrhizobiaceaeBradyrhizobium 228 Bacteria Proteobacteria AlphaproteobacteriaRhizobiales Bradyrhizobiaceae Bradyrhizobium 229 Bacteria ProteobacteriaAlphaproteobacteria Rhizobiales Rhizobiaceae Rhizobium 230 BacteriaProteobacteria Alphaproteobacteria Rhizobiales Rhizobiaceae Rhizobium231 Bacteria Proteobacteria Betaproteobacteria BurkholderialesBurkholderiaceae Polynucleobacter 232 Bacteria ProteobacteriaBetaproteobacteria Burkholderiales Burkholderiaceae Polynucleobacter 233Bacteria Proteobacteria Alphaproteobacteria Rhizobiales RhizobiaceaeRhizobium 234 Bacteria Bacteroidetes Sphingobacteriia SphingobacterialesChitinophagaceae Filimonas 235 Bacteria Bacteroidetes SphingobacteriiaSphingobacteriales Chitinophagaceae Filimonas 236 Bacteria BacteroidetesSphingobacteriia Sphingobacteriales Chitinophagaceae Filimonas 237Bacteria Proteobacteria Gammaproteobacteria XanthomonadalesXanthomonadaceae Dyella 238 Bacteria Proteobacteria GammaproteobacteriaEnterobacteriales Enterobacteriaceae Pantoea 239 Bacteria ProteobacteriaGammaproteobacteria Xanthomonadales Xanthomonadaceae Luteibacter 240Bacteria Proteobacteria Gammaproteobacteria XanthomonadalesXanthomonadaceae DyeIla 241 Bacteria Proteobacteria GammaproteobacteriaXanthomonadales Xanthomonadaceae Luteibacter 242 Bacteria ProteobacteriaBetaproteobacteria Burkholderiales Burkholderiaceae Ralstonia 243Bacteria Proteobacteria Gammaproteobacteria EnterobacterialesEnterobacteriaceae Erwinia 244 Bacteria Firmicutes Bacilli BacillalesBacillaceae Bacillus 245 Bacteria Firmicutes Bacilli BacillalesBacillaceae Bacillus 246 Bacteria Firmicutes Bacilli BacillalesBacillaceae Bacillus 247 Bacteria Firmicutes Bacilli BacillalesBacillaceae Bacillus 248 Bacteria Firmicutes Bacilli BacillalesPaenibacillaceae Paenibacillus 249 Bacteria ProteobacteriaGammaproteobacteria Enterobacteriales Enterobacteriaceae Pantoea

TABLE 2 Fungal host endophytes of the present invention SEQ ID KingdomPhylum Class Order Family Genus 250 Fungi Ascomycota PezizomycotinaSordariomycetes Xylariomycetidae Pestalotiopsis 251 Fungi AscomycotaEurotiomycetes Chaetothyriales Herpotrichiellaceae Phaeomoniella 252Fungi Ascomycota Sordariomycetes Sordariomycetes XylariomycetidaeBiscogniauxia 253 Fungi Ascomycota Eurotiomycetes ChaetothyrialesHerpotrichiellaceae Phaeomoniella 254 Fungi Ascomycota SordariomycetesSordariomycetes unidentified Sordariomycetes unidentifiedSordariomycetes unidentified 255 Fungi Ascomycota EurotiomycetesChaetothyriales Chaetothyriales unidentified Chaetothyrialesunidentified 256 Fungi Ascomycota Dothideomycetes Pleosporales Incertaesedis Phoma 257 Fungi Ascomycota Dothideomycetes PleosporalesPleosporaceae Alternaria 258 Fungi Ascomycota DothideomycetesDothideales Dothioraceae Aureobasidium 259 Fungi AscomycotaSordariomycetes Coniochaetales Coniochaetaceae Lecythophora 260 FungiAscomycota Dothideomycetes Dothideales Dothioraceae Hormonema 261 FungiAscomycota Dothideomycetes Pleosporales Sporormiaceae Preussia 262 FungiAscomycota Sordariomycetes Coniochaetales Coniochaetaceae Lecythophora263 Fungi Ascomycota Dothideomycetes Incertae sedis Incertae sedisMonodictys 264 Fungi Ascomycota Sordariomycetes XylarialesAmphisphaeriaceae Pestalotiopsis 265 Fungi Ascomycota DothideomycetesCapnodiales Mycosphaerellaceae Cladosporium 266 Fungi AscomycotaDothideomycetes Botryosphaeriales Botryosphaeriaceae Botryosphaeria 267Fungi Ascomycota Dothideomycetes Botryosphaeriales BotryosphaeriaceaePhyllosticta 268 Fungi Ascomycota Dothideomycetes PleosporalesMontagnulaceae Paraconiothyrium 269 Fungi Ascomycota SordariomycetesXylariales Amphisphaeriaceae Pestalotiopsis 270 Fungi AscomycotaDothideomycetes Pleosporales Montagnulaceae Paraconiothyrium 271 FungiAscomycota Eurotiomycetes Eurotiales Trichocomaceae Penicillium 272Fungi Ascomycota Sordariomycetes Xylariales Xylariaceae Xylariaceaeunidentified 273 Fungi Ascomycota Sordariomycetes Xylariales XylariaceaeXylariaceae unidentified 274 Fungi Ascomycota SordariomycetesSordariomycetes unidentified Sordariomycetes unidentifiedSordariomycetes unidentified 275 Fungi Ascomycota SordariomycetesXylariales Xylariaceae Xylariaceae unidentified 276 Fungi AscomycotaSordariomycetes Xylariales Xylariaceae Xylariaceae unidentified 277Fungi Ascomycota Sordariomycetes Hypocreales Nectriaceae Fusarium 278Fungi Ascomycota Sordariomycetes Hypocreales Nectriaceae Fusarium 279Fungi Ascomycota Sordariomycetes Hypocreales Nectriaceae Fusarium 280Fungi Ascomycota Sordariomycetes Hypocreales Nectriaceae Nectria 281Fungi Ascomycota Sordariomycetes Hypocreales Nectriaceae Fusarium 282Fungi Ascomycota Sordariomycetes Xylariales Xylariaceae Xylaria 283Fungi Ascomycota Sordariomycetes Xylariales Xylariaceae Hypoxylon 284Fungi Ascomycota Sordariomycetes Hypocreales Nectriaceae Fusarium 285Fungi Ascomycota Sordariomycetes Xylariales Xylariaceae Xylaria 286Fungi Ascomycota Sordariomycetes Xylariales Xylariaceae Xylaria 287Fungi Ascomycota Sordariomycetes Hypocreales Nectriaceae Fusarium 288Fungi Ascomycota Dothideomycetes Pleosporales Sporormiaceae Preussia 289Fungi Ascomycota Dothideomycetes Pleosporales Sporormiaceae Preussia 290Fungi Ascomycota Dothideomycetes Pleosporales Sporormiaceae Preussia 291Fungi Ascomycota Sordariomycetes Hypocreales Nectriaceae Fusarium 292Fungi Ascomycota Sordariomycetes Hypocreales Nectriaceae Fusarium 293Fungi Ascomycota Sordariomycetes Hypocreales Nectriaceae Fusarium 294Fungi Ascomycota Dothideomycetes Pleosporales Sporormiaceae Preussia 295Fungi Ascomycota Dothideomycetes Pleosporales MontagnulaceaeParaconiothyrium 296 Fungi Ascomycota Dothideomycetes PleosporalesMontagnulaceae Paraconiothyrium 297 Fungi Ascomycota DothideomycetesPleosporales Pleosporales unidentified Pleosporales unidentified 298Fungi Ascomycota Sordariomycetes Coniochaetales ConiochaetaceaeLecythophora 299 Fungi Ascomycota Dothideomycetes Pleosporales Incertaesedis Phoma 300 Fungi Ascomycota Sordariomycetes SordarialesSordariaceae Neurospora 301 Fungi Ascomycota DothideomycetesDothideomycetes unidentified Dothideomycetes unidentifiedDothideomycetes unidentified 302 Fungi Ascomycota DothideomycetesCapnodiales Davidiellaceae Cladosporium 303 Fungi AscomycotaDothideomycetes Pleosporales Sporormiaceae Preussia 304 Fungi AscomycotaDothideomycetes Capnodiales Davidiellaceae Cladosporium 305 FungiAscomycota Dothideomycetes Pleosporales Pleosporales Incertae sedisPericonia 306 Fungi Ascomycota Dothideomycetes Pleosporales PleosporalesIncertae sedis Periconia 307 Fungi Ascomycota DothideomycetesPleosporales Pleosporaceae Alternaria 308 Fungi AscomycotaDothideomycetes Pleosporales Pleosporales Incertae sedis Periconia 309Fungi Ascomycota Dothideomycetes Pleosporales Pleosporaceae Alternaria310 Fungi Ascomycota Dothideomycetes Pleosporales Pleosporales Incertaesedis Periconia 311 Fungi Ascomycota Dothideomycetes CapnodialesDavidiellaceae Cladosporium 312 Fungi Ascomycota DothideomycetesDothideales Dothideales unidentified Dothideales unidentified 313 FungiAscomycota Dothideomycetes Pleosporales Leptosphaeriaceae Coniothyrium314 Fungi Ascomycota Dothideomycetes Pleosporales PleosporaceaeAlternaria 315 Fungi Ascomycota Dothideomycetes PleosporalesPleosporaceae Alternaria 316 Fungi Ascomycota DothideomycetesPleosporales Pleosporales Incertae sedis Periconia 317 Fungi AscomycotaDothideomycetes Pleosporales Pleosporales Incertae sedis Periconia 318Fungi Ascomycota Dothideomycetes Capnodiales Davidiellaceae Cladosporium319 Fungi Ascomycota Dothideomycetes Pleosporales PleosporaceaeAlternaria 320 Fungi Ascomycota Dothideomycetes PleosporalesPleosporales Incertae sedis Periconia 321 Fungi AscomycotaDothideomycetes Pleosporales Sporormiaceae Preussia 322 Fungi AscomycotaDothideomycetes Pleosporales Sporormiaceae Sporormiaceae unidentified323 Fungi Ascomycota Dothideomycetes Pleosporales Sporormiaceae Preussia324 Fungi Ascomycota Dothideomycetes Pleosporales Sporormiaceae Preussia325 Fungi Ascomycota Dothideomycetes BotryosphaerialesBotryosphaeriaceae Botryosphaeria 326 Fungi Ascomycota DothideomycetesBotryosphaeriales Botryosphaeriaceae Microdiplodia 327 Fungi AscomycotaSordariomycetes Xylariales Amphisphaeriaceae Pestalotiposis 328 FungiAscomycota Dothideomycetes Botryosphaeriales BotryosphaeriaceaePhyllosticta 329 Fungi Ascomycota Dothideomycetes PleosporalesPleosporaceae Alternaria 330 Fungi Ascomycota SordariomycetesConiochaetales Coniochaetaceae Lecythophora 331 Fungi AscomycotaDothideomycetes Botryosphaeriales Botryosphaeriaceae Microdiplodia 332Fungi Ascomycota Sordariomycetes Xylariales Xylariaceae Daldinia 333Fungi Zygomycota Mucoromycotina Mucorales Mucoraceae Mucor

TABLE 3 Examples of Complex Endophytes The following fungi andassociated bacteria are examples of complex endophytes. These complexendophytes and their components are contemplated to be examples ofuseful compositions of the present invention. Fungal Host EndofungalBacterium Reference Rhizopus Burkholderia Partida-Martinez L P, HertweckC. 2005. Pathogenic fungus microsporus rhizoxinica harboursendosymbiotic bacteria for toxin production. Nature 437: 884-888. doi:10.1038/nature03997 Aspergillus Streptomyces Schroeckh V, et al. (2009)Intimate bacterial-fungal interaction nidulans rapamycinicus triggersbiosynthesis of archetypal polyketides in Aspergillus nidulans. ProcNatl Acad Sci USA 106: 14558-14563. Gigaspora Candidatus Bianciotto V,Lumini E, Lanfranco L, Minerdi D, Bonfante P, et al. margaritaGlomeribacter 2000. Detection and identification of bacterialendosymbionts in (mycorrhiza) gigasporarum (related arbuscularmycorrhizal fungi belonging to the family Gigasporaceae. toBurkholderia) Appl. Environ. Microbiol. 66: 4503-9 PiriformosporaRhizobium radiobacter Sharma M, Schmid M, Rothballer M, Hause G, ZuccaroA, et al. indica (synonym of 2008. Detection and identification ofbacteria intimately Agrobacterium associated with fungi of the orderSebacinales. Cell Microbiol. tumefaciens) 10: 2235-46 LaccariaPaenibacillus spp. Bertaux J, Schmid M, Prevost-Boure N C, Churin J L,Hartmann A, bicolor et al. 2003. In situ identification of intracellularbacteria related to Paenibacillus spp. in the mycelium of theectomycorrhizal fungus Laccaria bicolor S238N. Appl. Environ. Microbiol.69: 4243-48 Tuber borchii Cytophaga- Barbieri E, Potenza L, Rossi I,Sisti D, Giomaro G, et al. 2000. Flexibacter- Phylogeneticcharacterization and in situ detection of a BacteroidesCytophaga-Flexibacter-Bacteroides phylogroup bacterium in (Cytophagales)Tuber borchii Vittad. ectomycorrhizal mycelium. Appl. Environ.Microbiol. 66: 5035-42 Pestalotiposis Luteibacter sp. Hoffman M T,Gunatilaka M K, Wijeratne K, Gunatilaka L, Arnold sp. A E (2013)Endohyphal Bacterium Enhances Production of Indole- 3-Acetic Acid by aFoliar Fungal Endophyte. PLoS ONE 8(9): e73132. doi:10.1371/journal.pone.0073132 Mucor sp. Pantoea sp. unpublished

TABLE 4 Complex Endophytes and Complex Endophyte Components tested inthe present invention The following endophytes (complex endophytes andtheir corresponding component bacteria) were used as exemplaryendophytes in the methods described in the Examples section. Thesecomplex endophytes and their components are contemplated to be examplesof useful compositions of the present invention. ID Description SequenceIdentifier SYM16668 Complex endophyte fungal host Fungal host ITS: SEQIDNO: 325 further comprising SYM16658 (Genus Botryosphaeria) SYM16669Complex endophyte fungal host Fungal host ITS: SEQID NO: 326 furthercomprising SYM16659 (Genus Microdiplodia) SYM16670 Complex endophytefungal host Fungal host ITS: SEQID NO: 327 (SYM166) further comprisingSYM16660 (Genus Pestalotiposis) SYM16671 Complex endophyte fungal hostFungal host ITS: SEQID NO: 328 further comprising SYM16661 (GenusPhyllosticta) SYM16672 Complex endophyte fungal host Fungal host LSU:SEQID NO: 329 further comprising SYM16662 (Genus Alternaria) SYM16673Complex endophyte fungal host Fungal host ITS: SEQID NO: 330 furthercomprising SYM16663 (Genus Lecythophora) SYM16674 Complex endophytefungal host Fungal host ITS: SEQID NO: 331 further comprising SYM16665(Genus Microdiplodia) SYM16675 Complex endophyte fungal host Fungal hostITS: SEQID NO: 332 further comprising SYM16666 (Genus Daldinia) SYM16658Bacterial component of Bacterial component 16S: SEQID NO: 237 complexendophyte SYM16668 (Genus Dyella) SYM16659 Bacterial component ofBacterial component 16S: SEQID NO: 238 complex endophyte SYM16669 (GenusPantoea) SYM16660 Bacterial component of Bacterial component 16S: SEQIDNO: 239 complex endophyte SYM16670 (Genus Luteibacter) SYM16661Bacterial component of Bacterial component 16S: SEQID NO: 240 complexendophyte SYM16671 (Genus Dyella) SYM16662 Bacterial component ofBacterial component 16S: SEQID NO: 241 complex endophyte SYM16672 (GenusLuteibacter) SYM16663 Bacterial component of Bacterial component 16S:SEQID NO: 242 complex endophyte SYM16673 (Genus Ralstonia) SYM16665Bacterial component of Bacterial component 16S: SEQID NO: 243 complexendophyte SYM16674 (Genus Erwinia) SYM16666 Bacterial component ofBacterial component 16S: SEQID NO: 244 complex endophyte SYM16675 (GenusBacillus)

TABLE 5 Soybean Seedling Germination Water (Drought) Stress AssayComplex endophytes and their isolated bacterial endophyte componentswere compared to each other as well as to control solutions (fungalformulation for the complex endophytes and bacterial formulation for theisolated bacterial endophyte components, respectively) and non-treated,for their ability to improve germination rates in soybean seeds. Complexendophyte treatment improves germination rate of soybean seedlings underdrought (water stressed) conditions vs. formulation controls.Dothideomycetes (D) as complex endophyte hosts appear to impart greaterbenefit to soybean seedling germination under water stress (droughtstress) conditions vs. their isolated bacterial components, than doSodariomycetes (S). % Germination of soybean seedlings Complex EndophyteEndofungal Bacterial Endophyte SYM16668 (D) 53.33% 70.00% SYM16658SYM16669 (D) 63.33% 33.33% SYM16659 SYM16670 (S) 20.00% 56.67% SYM16660SYM16671 (D) 60.00% 23.33% SYM16661 SYM16672 (D) 40.00% 23.33% SYM16662SYM16673 (S) 10.00% 36.67% SYM16663 SYM16674 (D) 53.33% 33.33% SYM16665SYM16675 (S) 30.00% 80.00% SYM16666 Average 41.25% 44.58% Average Fungal13.33% 53.33% Bacterial Formulation Formulation Control Control D =Dothideomycetes S = Sodariomycetes

TABLE 6 Wheat Seedling Germination Water (Drought) Stress Assay Complexendophytes and their isolated bacterial endophyte components werecompared to each other as well as to control solutions (fungalformulation for the complex endophytes and bacterial formulation for theisolated bacterial endophyte components, respectively) and non-treated,for their ability to improve germination rates in wheat seeds. Complexendophyte treatment, as well as bacterial endohpyte treatment, improvesgermination rate of wheat seedlings under drought (water stressed)conditions vs. formulation controls. Sodariomycetes (S) as complexendophyte hosts appear to impart greater benefit to soybean seedlinggermination under water stress (drought stress) conditions vs. theirisolated bacterial components, than do Dothideomycetes (D). %Germination of wheat seedlings Complex Endophyte Endofungal BacterialEndophyte SYM16668 (D) 35.56% 53.33% SYM16658 SYM16669 (D) 68.89% 68.89%SYM16659 SYM16670 (S) 42.22% 40.00% SYM16660 SYM16671 (D) 42.22% 48.89%SYM16661 SYM16672 (D) 46.67% 48.89% SYM16662 SYM16673 (S) 64.44% 55.56%SYM16663 SYM16674 (D) 53.33% 55.56% SYM16665 SYM16675 (S) 55.56% 40.00%SYM16666 Average 51.11% 51.39% Average Fungal 42.22% 44.44% BacterialFormulation Formulation Control Control D = Dothideomycetes S =Sodariomycetes

TABLE 7 Wheat Plant Vigor Assay: Non-Stressed Conditions Table 7a: RootLength Plant seedlings grown from seeds treated with complex endophytesor complex endophyte bacterial components display a greater average rootlength than do plant seedlings grown from seeds treated with theformulation control. No significant difference was observed in averageroot length between plants grown from seeds treated with complexendophytes vs. isolated bacterial components. Average root length (cm)Complex Formulation Bacterial Endophyte Control = 14.48 Component SYM16668 16.53 15.87 SYM 16658 SYM 16669 18.23 15.75 SYM 16659 SYM 1667015.48 16.15 SYM 16660 SYM 16671 14.32 17.09 SYM 16661 SYM 16672 17.3817.90 SYM 16662 SYM 16673 17.14 17.72 SYM 16663 SYM 16674 16.68 17.02SYM 16665 SYM 16675 16.00 14.42 SYM 16666 Average 16.47 16.49 AverageTable 7b: Shoot Length Plant seedlings grown from seeds treated withcomplex endophytes or complex endophyte bacterial components display agreater average shoot length than do plant seedlings grown from seedstreated with the formulation control. Plant seedlings grown from seedstreated with complex endophytes display a greater average shoot lengththan do plant seedlings grown from seeds treated with isolated bacterialcomponents. Average shoot length (cm) Complex Formulation BacterialEndophyte Control = 14.31 Component SYM 16668 15.74 14.11 SYM 16658 SYM16669 16.77 15.38 SYM 16659 SYM 16670 16.88 15.03 SYM 16660 SYM 1667117.19 14.79 SYM 16661 SYM 16672 15.48 15.20 SYM 16662 SYM 16673 14.9814.32 SYM 16663 SYM 16674 14.52 15.07 SYM 16665 SYM 16675 14.30 15.66SYM 16666 Average 15.73 14.94 Average Table 7c: Seedling Mass Averagemass of seedlings grown from seeds treated with the endophytecompositions listed below, compared to seedlings grown from seedstreated with only the formulation control. Average total mass ofTreatment seedlings (g) Formulation 2.70 SYM 16658 2.89 SYM 16659 2.75SYM 16660 2.40 SYM 16661 2.48 SYM 16662 1.91 SYM 16663 2.46 SYM 166652.08 SYM 16666 2.78 SYM 16668 2.17 SYM 16669 2.73 SYM 16670 2.96 SYM16671 2.97 SYM 16672 2.67 SYM 16673 2.06 SYM 16674 2.19 SYM 16675 2.20

TABLE 8 Wheat Plant Vigor Assay: Water-Stressed (Drought) ConditionsTable 8a: Root Length Plant seedlings grown from seeds treated withcomplex endophytes or complex endophyte bacterial components display agreater average root length than do plant seedlings grown from seedstreated with the formulation control. No significant difference wasobserved between plants grown from seeds treated with complex endophytesvs. isolated bacterial components. Average root length (cm) ComplexFormulation Bacterial Endophyte Control = 12.83 Component 15.87 SYM16658 SYM 16669 14.24 13.02 SYM 16659 SYM 16670 13.10 13.10 SYM 16660SYM 16671 11.20 14.50 SYM 16661 SYM 16672 13.35 14.22 SYM 16662 SYM16673 16.97 16.04 SYM 16663 SYM 16674 13.97 14.15 SYM 16665 SYM 1667515.52 12.75 SYM 16666 Average 14.05 14.21 Average Table 8b: Shoot LengthPlant seedlings grown from seeds treated with complex endophytes orcomplex endophyte bacterial components display a greater average shootlength than do plant seedlings grown from seeds treated with theformulation control. Plant seedlings grown from seeds treated withcomplex endophytes display a greater average shoot length than do plantseedlings grown from seeds treated with isolated bacterial components.Average shoot length (cm) Complex Formulation Bacterial EndophyteControl = 9.77 Component 12.62 SYM 16658 SYM 16669 12.59 11.27 SYM 16659SYM 16670 11.94 9.10 SYM 16660 SYM 16671 10.33 10.50 SYM 16661 SYM 1667212.63 9.45 SYM 16662 SYM 16673 11.22 10.51 SYM 16663 SYM 16674 10.379.72 SYM 16665 SYM 16675 10.35 10.60 SYM 16666 Average 11.35 10.47Average Table 8c: Seedling Mass Average mass of seedlings grown fromseeds treated with the endophyte compositions listed below, compared toseedlings grown from seeds treated with only the formulation control.Average total mass of Treatment seedlings (g) Formulation 1.095 SYM16658 1.77 SYM 16659 1.01 SYM 16660 0.72 SYM 16661 0.765 SYM 16662 0.56SYM 16663 0.765 SYM 16665 0.555 SYM 16666 0.945 SYM 16669 1.15 SYM 166700.92 SYM 16671 0.95 SYM 16672 1.05 SYM 16673 0.895 SYM 16674 0.855 SYM16675 0.68

TABLE 9 Soybean Plant Vigor Assay: Non-Stressed Conditions Table 9a:Root Length Plant seedlings grown from seeds treated with complexendophytes or complex endophyte bacterial components display a greateraverage root length than do plant seedlings grown from seeds treatedwith the formulation control. Plant seedlings grown from seeds treatedwith complex endophytes display a greater average root length than doplant seedlings grown from seeds treated with isolated bacterialcomponents. Average root length (cm) Complex Formulation BacterialEndophyte Control = 14.21 Component SYM 16668 19.30 17.36 SYM 16658 SYM16669 18.00 18.06 SYM 16659 SYM 16670 14.00 17.90 SYM 16660 SYM 1667120.96 21.00 SYM 16661 SYM 16672 18.33 16.00 SYM 16662 SYM 16673 18.4014.40 SYM 16663 SYM 16674 20.86 19.51 SYM 16665 SYM 16675 21.47 20.00SYM 16666 Average 18.92 18.03 Average Table 9b: Shoot Length Plantseedlings grown from seeds treated with complex endophytes or complexendophyte bacterial components display a greater average shoot lengththan do plant seedlings grown from seeds treated with the formulationcontrol. Plant seedlings grown from seeds treated with isolatedbacterial components display a slightly greater average shoot lengththan do plant seedlings grown from seeds treated with the complexendophytes. Average shoot length (cm) Complex Formulation BacterialEndophyte Control = 5.75 Component SYM 16668 7.56 6.52 SYM 16658 SYM16669 7.50 8.54 SYM 16659 SYM 16670 9.00 7.53 SYM 16660 SYM 16671 6.758.35 SYM 16661 SYM 16672 7.44 6.67 SYM 16662 SYM 16673 6.10 7.00 SYM16663 SYM 16674 5.54 7.88 SYM 16665 SYM 16675 6.17 7.14 SYM 16666Average 7.01 7.45 Average Table 9c: Seedling Mass Average mass ofseedlings grown from seeds treated with the endophyte compositionslisted below, compared to seedlings grown from seeds treated with onlythe formulation control. Average total mass Treatment of seedlings (g)SYM 16668 8.645 SYM 16658 10.7425 SYM 16669 9.6485 SYM 16659 9.0095 SYM16670 8.198 SYM 16660 10.536 SYM 16671 9.411 SYM 16661 12.664 SYM 1667210.7265 SYM 16662 7.516 SYM 16673 10.9655 SYM 16663 7.911 SYM 1667412.0485 SYM 16665 9.407 SYM 16675 13.637 SYM 16666 12.0625 Formulation10.385

TABLE 10 Soybean Plant Vigor Assay: Water-Stressed (Drought) ConditionsTable 10a: Root Length Plant seedlings grown from seeds treated with acomplex endophyte or complex endophyte bacterial component display agreater average root length than do plant seedlings grown from seedstreated with the formulation control. Plant seedlings grown from seedstreated with complex endophytes display a greater average root lengththan do plant seedlings grown from seeds treated with isolated bacterialcomponents. Average root length (cm) Complex Formulation BacterialEndophyte Control = 15.67 Component SYM 16668 19.12 16.06 SYM 16658 SYM16669 17.98 16.46 SYM 16659 SYM 16670 15.89 16.81 SYM 16660 SYM 1667116.03 17.16 SYM 16661 SYM 16672 14.60 14.50 SYM 16662 SYM 16673 19.0314.00 SYM 16663 SYM 16674 16.07 15.63 SYM 16665 SYM 16675 17.79 16.01SYM 16666 Average 17.06 15.83 Average Table 10b: Shoot Length Plantseedlings grown from seeds treated with complex endophytes or complexendophyte bacterial components display a greater average shoot lengththan do plant seedlings grown from seeds treated with the formulationcontrol. No significant difference was observed between plants grownfrom seeds treated with complex endophytes vs. isolated bacterialcomponents. Average shoot length (cm) Complex Formulation BacterialEndophyte Control = 3.69 Component SYM 16668 5.49 5.00 SYM 16658 SYM16669 4.38 5.09 SYM 16659 SYM 16670 4.70 6.60 SYM 16660 SYM 16671 6.156.64 SYM 16661 SYM 16672 5.95 4.75 SYM 16662 SYM 16673 4.71 5.08 SYM16663 SYM 16674 5.88 4.55 SYM 16665 SYM 16675 4.69 4.63 SYM 16666Average 5.24 5.29 Average Table 10c: Seedling Mass Average mass ofseedlings grown from seeds treated with the endophyte compositionslisted below, compared to seedlings grown from seeds treated with onlythe formulation control. Average total mass of Treatment seedlings (g)SYM 16668 5.1394 SYM 16658 7.07565 SYM 16669 7.37525 SYM 16659 6.1235SYM 16670 5.9322 SYM 16660 4.22315 SYM 16671 4.2446 SYM 16661 4.367 SYM16672 4.0583 SYM 16662 4.94655 SYM 16673 5.27775 SYM 16663 5.431 SYM16674 5.0386 SYM 16665 4.911 SYM 16675 6.5926 SYM 16666 2.49395Formulation 5.4958

TABLE 11 Winter Wheat Field Trial Results Winter wheat grown undernon-irrigated (dryland) conditions from winter wheat (Variety 3) seedstreated with complex endophyte SYM166 demonstrate improved yield (bothwet bushels per acre and dry bushels per acre) compared to seeds treatedwith either the fungal formulation control or with non-complex fungalendophytes. Yield (Winter Wheat Variety 3) Dry Bushels Wet Bushels perAcre per Acre SYM166 (Complex Endophyte) 37.24 33.70 Average of FungalEndophyte 29.80 28.47 Controls (non-Complex) Fungal Formulation Control26.52 25.32

TABLE 12 Spring Wheat Field Trial Results Spring wheat grown undernon-irrigated (dryland) conditions from winter wheat (Variety 2) seedstreated with complex endophyte SYM166 demonstrate improved yield (bothwet bushels per acre and dry bushels per acre) compared to seeds treatedwith either the fungal formulation control or with non-complex fungalendophytes. Yield (Spring Wheat Variety 2) Dry Bushels Wet Bushels perAcre per Acre SYM166 (Complex Endophyte) 46.56 49.96 Average of FungalEndophyte 45.23 48.08 Controls (non-Complex) Fungal Formulation Control42.92 41.12

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1.-102. (canceled)
 103. A synthetic composition, comprising a plantelement heterologously associated with an endophytic component, whereinsaid endophyte comprises a nucleic acid sequence at least 97% identicalto SEQ ID NO: 333 and is capable of providing a trait of agronomicimportance to said plant element.
 104. The synthetic composition ofclaim 103, wherein said trait of agronomic importance is selected fromthe group consisting of: germination rate, emergence rate, shootbiomass, seedling root length, seedling shoot length, seedling mass,root surface area, enhanced nutrient use efficiency, and yield.
 105. Thesynthetic composition of claim 104, wherein the trait of agronomicimportance is improved under normal watering conditions.
 106. Thesynthetic composition of claim 104, wherein the trait of agronomicimportance is improved under normal watering conditions.
 107. Thesynthetic composition of claim 103, wherein said synthetic compositionfurther comprises an agronomic formulation that further comprises one ormore of the following: a stabilizer, or a preservative, or a carrier, ora surfactant, or an anticomplex agent, fungicide, nematicide,bactericide, insecticide, and herbicide, or any combination thereof.108. The synthetic composition of claim 103, wherein said endophyte ispresent in an amount of at least about 10{circumflex over ( )}2 CFU perplant element.
 109. The synthetic composition of claim 103, wherein saidplant element is selected from the group consisting of: whole plant,seedling, meristematic tissue, ground tissue, vascular tissue, dermaltissue, seed, leaf, root, shoot, stem, flower, fruit, stolon, bulb,tuber, corm, keikis, and bud.
 110. The synthetic composition of claim103, wherein said plant element is from a plant selected from the groupconsisting of: wheat, soybean, maize, cotton, canola, barley, sorghum,millet, rice, rapeseed, alfalfa, tomato, sugarbeet, sorghum, almond,walnut, apple, peanut, strawberry, lettuce, orange, potato, banana,sugarcane, potato, cassava, mango, guava, palm, onions, olives, peppers,tea, yams, cacao, sunflower, asparagus, carrot, coconut, lemon, lime,barley, watermelon, cabbage, cucumber, grape, and turfgrass.
 111. Amethod of inoculating a plant with a synthetic composition, comprisingcontacting a plant element of said plant with a formulation comprising aheterologous endophyte, wherein said endophyte comprises a nucleic acidsequence at least 97% identical to SEQ ID NO: 333 and the endophyte isheterologously disposed to the plant element in an amount effective toimprove a trait of agronomic compared to a reference plant grown underthe same conditions.
 112. The method of claim 111, wherein said trait ofagronomic importance is selected from the group consisting of:germination rate, emergence rate, shoot biomass, seedling root length,seedling shoot length, seedling mass, root surface area, enhancednutrient use efficiency, and yield.
 113. The method of claim 112,wherein the trait of agronomic importance is improved under normalwatering conditions.
 114. The method of claim 112, wherein the trait ofagronomic importance is improved under conditions of water limitation.115. The method of claim 111, wherein said synthetic composition furthercomprises an agronomic formulation that further comprises one or more ofthe following: a stabilizer, or a preservative, or a carrier, or asurfactant, or an anticomplex agent, fungicide, nematicide, bactericide,insecticide, and herbicide, or any combination thereof.
 116. The methodof claim 111, wherein said endophyte is present in an amount of at leastabout 10{circumflex over ( )}2 CFU per plant element.
 117. The method ofclaim 111, wherein said plant element is selected from the groupconsisting of: whole plant, seedling, meristematic tissue, groundtissue, vascular tissue, dermal tissue, seed, leaf, root, shoot, stem,flower, fruit, stolon, bulb, tuber, corm, keikis, and bud.
 118. Themethod of claim 111, wherein said plant element is from a plant selectedfrom the group consisting of: wheat, soybean, maize, cotton, canola,barley, sorghum, millet, rice, rapeseed, alfalfa, tomato, sugarbeet,sorghum, almond, walnut, apple, peanut, strawberry, lettuce, orange,potato, banana, sugarcane, potato, cassava, mango, guava, palm, onions,olives, peppers, tea, yams, cacao, sunflower, asparagus, carrot,coconut, lemon, lime, barley, watermelon, cabbage, cucumber, grape, andturfgrass.